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humans (131) 131
male (100) 100
female (78) 78
hematology (49) 49
adult (45) 45
hemophilia a - genetics (40) 40
hemophilia (39) 39
hemophilia a - ethnology (34) 34
homosexuality (34) 34
index medicus (34) 34
hemophilia a - complications (31) 31
acquired immunodeficiency syndrome - epidemiology (30) 30
haiti - ethnology (29) 29
adolescent (27) 27
factor viii - genetics (27) 27
risk (27) 27
factor ix - genetics (26) 26
united states (25) 25
child (23) 23
middle aged (23) 23
mutation (23) 23
hemophilia b - genetics (21) 21
hemophilia b - ethnology (19) 19
alleles (17) 17
dna mutational analysis (17) 17
risk factors (17) 17
hemophilia a - immunology (16) 16
polymerase chain reaction (16) 16
polymorphism, restriction fragment length (16) 16
child, preschool (15) 15
infant (15) 15
substance-related disorders - complications (15) 15
base sequence (14) 14
gene frequency (14) 14
molecular sequence data (14) 14
pedigree (14) 14
young adult (14) 14
aids (13) 13
blood coagulation factor viii (12) 12
genetic aspects (12) 12
genetics & heredity (12) 12
acquired immunodeficiency syndrome - etiology (11) 11
european continental ancestry group - genetics (11) 11
factor viii - immunology (11) 11
factor-viii gene (11) 11
hemophilia a (11) 11
hemophilia a - drug therapy (11) 11
polymorphisms (11) 11
pregnancy (11) 11
acquired immunodeficiency syndrome - transmission (10) 10
genotype (10) 10
haplotypes (10) 10
acquired immunodeficiency syndrome - immunology (9) 9
europe (9) 9
factor ix (9) 9
factor viii (9) 9
haemophilia (9) 9
hemophilia a - therapy (9) 9
hemophilia b - diagnosis (9) 9
heterozygote (9) 9
infant, newborn (9) 9
inhibitors (9) 9
mutations (9) 9
peripheral vascular disease (9) 9
sarcoma, kaposi - epidemiology (9) 9
sexual behavior (9) 9
transfusion reaction (9) 9
acquired immunodeficiency syndrome - mortality (8) 8
china - ethnology (8) 8
factor viii - therapeutic use (8) 8
genes (8) 8
hemophilia a - diagnosis (8) 8
introns - genetics (8) 8
previously untreated patients (8) 8
severity of illness index (8) 8
africa - ethnology (7) 7
aged (7) 7
blood transfusion (7) 7
dna (7) 7
epidemiologic methods (7) 7
epidemiology (7) 7
european continental ancestry group (7) 7
gene (7) 7
genetic research (7) 7
health aspects (7) 7
hemophilia a - epidemiology (7) 7
hemophilia b (7) 7
polymorphism, genetic (7) 7
population (7) 7
prevalence (7) 7
age factors (6) 6
analysis (6) 6
antibodies, viral - analysis (6) 6
cohort studies (6) 6
disease (6) 6
diseases (6) 6
ethnic groups (6) 6
exons - genetics (6) 6
factor viii - antagonists & inhibitors (6) 6
families (6) 6
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21. Full Text Haemostasis biomarkers and risk of intracerebral haemorrhage in the REasons for Geographic and Racial Differences in Stroke Study
by Zakai, Neil A and Olson, Nels C and Judd, Suzanne E and Kleindorfer, Dawn O and Kissela, Brett M and Howard, George and Cushman, Mary
Thrombosis and Haemostasis, ISSN 0340-6245, 2017, Volume 117, Issue 9, pp. 1808 - 1815
Summary Pathologic alterations in haemostasis cause bleeding disorders, but it is unknown if variation within the normal range relates to intracerebral... 
Stroke, Systemic or Venous Thromboembolism | Cerebral haemorrhage | Haemostasis | Epidemiology | Continental population groups | Cohort studies | SYSTEM | POPULATION | VENOUS THROMBOSIS | continental population groups | ATRIAL-FIBRILLATION | HEMOPHILIA | epidemiology | WARFARIN | haemostasis | cohort studies | PERIPHERAL VASCULAR DISEASE | COHORT | HEMATOLOGY | ASSOCIATION | Predictive Value of Tests | United States - epidemiology | Prognosis | Prospective Studies | Fibrin Fibrinogen Degradation Products - metabolism | Humans | Middle Aged | Stroke - diagnosis | African Americans | Male | Cerebral Hemorrhage - diagnosis | Cerebral Hemorrhage - blood | Time Factors | Hemostasis | Factor IX - metabolism | Female | Cerebral Hemorrhage - ethnology | Risk Factors | Proportional Hazards Models | Biomarkers - blood | Chi-Square Distribution | Stroke - blood | Stroke - ethnology | Aged | Nonlinear Dynamics | Cerebral Haemorrhage | Continental Population Groups | Cohort Studies
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22. Full Text ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency families
by Nichols, William C and Terry, Valeri H and Wheatley, Matthew A and Yang, Angela and Zivelin, Ariella and Ciavarella, Nicola and Stefanile, Caterina and Matsushita, Tadashi and Saito, Hidehiko and De Bosch, Norma B and Ruiz-Saez, Arlette and Torres, Argimiro and Thompson, Arthur R and Feinstein, Donald I and White, Gilbert C and Negrier, Claude and Vinciguerra, Christine and Aktan, Melih and Kaufman, Randal J and Ginsburg, David and Seligsohn, Uri
Blood, ISSN 0006-4971, 04/1999, Volume 93, Issue 7, pp. 2261 - 2266
Combined factors V and VIII deficiency is an autosomal recessive bleeding disorder associated with plasma levels of coagulation factors V and VIII... 
LEGUMINOUS LECTINS | GOLGI-APPARATUS | ENDOPLASMIC-RETICULUM | IDENTIFICATION | COMPARTMENT | HEMATOLOGY | SECRETORY PATHWAY | Haplotypes | Sequence Deletion | Genes | Humans | Male | Jews - genetics | Membrane Proteins - deficiency | DNA Mutational Analysis | Cloning, Molecular | Polymerase Chain Reaction | Female | Genetic Linkage | Introns - genetics | Factor V Deficiency - ethnology | Mannose-Binding Lectins | Factor V Deficiency - genetics | Membrane Proteins - genetics | Hemophilia A - ethnology | Exons - genetics | Genotype | Chromosomes, Bacterial | Genes, Recessive | Genetic Heterogeneity | Hemophilia A - complications | Point Mutation | Pedigree | Factor V Deficiency - complications | Hemophilia A - genetics | Mutation | Amino Acid Substitution
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23. Full Text The molecular genetic analysis of hemophilia A: A directed search strategy for the detection of point mutations in the human factor VIII gene
by Pattinson, J.K and Millar, D.S and McVey, J.H and Grundy, C.B and Wieland, K and Mibashan, R.S and Martinowitz, U and Tan-Un, K and Vidaud, M and Goossens, M and Sampietro, M and Mannucci, P.M and Krawczak, M and Reiss, J and Zoll, B and Whitmore, D and Bowcock, S and Wensley, R and Ajani, A and Mitchell, V and Rizza, C and Maia, R and Winter, P and Mayne, E.E and Schwartz, M and Green, P.J and Kakkar, V.V and Tuddenham, E.G.D and Cooper, D.N
Blood, ISSN 0006-4971, 12/1990, Volume 76, Issue 11, pp. 2242 - 2248
A directed-search strategy for point mutations in the factor VIII gene causing hemophilia A was used to screen eight potentially hypermutable CpG dinucleotides... 
China - ethnology | Nucleic Acid Hybridization | Pakistan - ethnology | Hemophilia A - ethnology | Humans | Factor VIII - genetics | Molecular Sequence Data | India - ethnology | Europe - ethnology | Israel - ethnology | DNA - genetics | Codon | Polymorphism, Restriction Fragment Length | Base Sequence | Polymerase Chain Reaction | Hemophilia A - genetics | Mutation
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24. Full Text The correlation between gene mutations and inhibitor development in patients with haemophilia A in southern Iran
by HAGHPANAH, S and SAHRAIIAN, M and AFRASIABI, A and ENAYATI, S and PEYVANDI, F and KARIMI, M
Haemophilia, ISSN 1351-8216, 09/2011, Volume 17, Issue 5, pp. 820 - 821
HEMATOLOGY | Severity of Illness Index | Genetic Predisposition to Disease - genetics | Introns - genetics | Hemophilia A - ethnology | Hemophilia A - immunology | Humans | Child, Preschool | Factor VIII - genetics | Exons - genetics | Male | Mutation - genetics | Blood Coagulation Factor Inhibitors - blood | Young Adult | Iran | DNA Mutational Analysis | Adolescent | Factor VIII - antagonists & inhibitors | Adult | Hemophilia A - genetics | Child | Genetic research | Care and treatment | Genetic aspects | Universities and colleges | Gene mutations | Hemophilia
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25. Factor IX mutations in haemophilia B patients in Malaysia: A preliminary study
by Balraj, Pauline and Ahmad, Munirah and Khoo, Alan Soo Beng and Ayob, Yasmin
Malaysian Journal of Pathology, ISSN 0126-8635, 06/2012, Volume 34, Issue 1, pp. 67 - 69
Haemophilia B is caused by coagulation defects in the factor IX gene located in Xq27.1 on the X chromosome. Identification of mutations contributing to... 
Hemophilia B | Clotting factor | Factor IX | Mutation | Severity of Illness Index | China - ethnology | Hemophilia B - diagnosis | Frameshift Mutation | Factor IX - analysis | Humans | Factor IX - genetics | Family Health | India - ethnology | Male | Hemophilia B - genetics | Mutation, Missense | Point Mutation | DNA Mutational Analysis | Malaysia - ethnology | Female | Hemophilia B - ethnology | Siblings
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26. Full Text Molecular genotyping of hemophilia A in Saudi Arabia: report of 2 novel mutations
by Owaidah, Tarek M and Alkhail, Hala Aba and Zahrani, Hazzaa Al and Musa, Abdulrahaman Al and Saleh, Mahasen Al and Riash, Mahmoud Abu and Alodaib, Ali and Amero, Khalid Abu
Blood Coagulation & Fibrinolysis, ISSN 0957-5235, 09/2009, Volume 20, Issue 6, pp. 415 - 418
Different types of mutations have been reported in patients with hemophilia A. Although about half of all severe factor VIII deficiencies are caused by gene... 
Genotype | Saudi | Arab and inhibitor | Hemophilia A | hemophilia A | MULTIPLEX PCR | PHENOTYPE | FACTOR-VIII GENE | SPECTRUM | IDENTIFICATION | HEMATOLOGY | genotype | INVERSIONS | Factor XII - immunology | Sequence Deletion | Factor XII - genetics | Frameshift Mutation | Introns - genetics | Hemophilia A - ethnology | Humans | Male | Codon, Nonsense | Mutation, Missense | Young Adult | Autoantibodies - immunology | Phenotype | DNA Mutational Analysis | Adolescent | Arabs - genetics | Isoantibodies - immunology | Adult | Hemophilia A - genetics | Mutagenesis, Insertional | Saudi Arabia - epidemiology | Index Medicus
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27. Carrier analysis for hemophilia a: Ideal versus acceptable
by Husain, Nuzhat
Expert Review of Molecular Diagnostics, ISSN 1473-7159, 04/2009, Volume 9, Issue 3, pp. 203 - 207
FRAGMENT-LENGTH-POLYMORPHISMS | INVERSION HOTSPOT | MOLECULAR DIAGNOSIS | CENTER DOCTORS ORGANIZATION | INDIAN POPULATION | FACTOR-VIII GENE | LINKAGE ANALYSIS | PATHOLOGY | DNA ANALYSIS | PRENATAL-DIAGNOSIS | C-GENE | Hemophilia A - ethnology | Humans | Factor VIII - genetics | Male | Genetic Counseling | Hemophilia A - metabolism | Polymorphism, Restriction Fragment Length | DNA Mutational Analysis | Polymerase Chain Reaction | Female | Heterozygote | Hemophilia A - genetics | Hemophilia A - diagnosis | Genetic Linkage
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28. Full Text Spectrum of factor VIII mutations in Arab patients with severe haemophilia A
by ABU‐AMERO, K. K and HELLANI, A and AL‐MAHED, M and AL‐SHEIKH, I
Haemophilia, ISSN 1351-8216, 05/2008, Volume 14, Issue 3, pp. 484 - 488
Haemophilia A is an X‐linked recessive bleeding disorder caused by mutations in the factor VIII (FVIII) gene. The mutation spectrum is known in various... 
factor VIII gene | mutation | intron 22 | haemophilia A | Arab | sequencing | Intron 22 | Haemophilia A | Mutation | Ffactor VIII gene | Sequencing | HEMATOLOGY | Severity of Illness Index | Introns - genetics | Prevalence | Hemophilia A - ethnology | Humans | Factor VIII - genetics | Male | Mutation - genetics | Middle East - epidemiology | Phenotype | DNA Mutational Analysis | Polymerase Chain Reaction | Arabs - genetics | Hemophilia A - genetics | Chromosome Inversion - genetics | Genetic aspects | Blood coagulation factor VIII | Hemophilia
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29. Full Text Characteristics of Persons With Heterosexually Acquired HIV Infection, United States 1999-2004
by Espinoza, Lorena and Hall, H. Irene and Hardnett, Felicia and Selik, Richard M and Ling, Qiang and Lee, Lisa M
American Journal of Public Health, ISSN 0090-0036, 01/2007, Volume 97, Issue 1, pp. 144 - 149
Objectives. In the United States a growing proportion of cases of heterosexually acquired HIV infections occur in women and in persons of color. We analyzed... 
SURVIVAL | DIAGNOSIS | WOMEN | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | ADOLESCENTS | RISK | AIDS | POPULATIONS | HUMAN-IMMUNODEFICIENCY-VIRUS | AFRICAN-AMERICAN | CARE | United States - epidemiology | Prevalence | Asian Americans - statistics & numerical data | Heterosexuality | HIV Infections - epidemiology | Humans | Middle Aged | Acquired Immunodeficiency Syndrome - psychology | HIV Infections - psychology | Hispanic Americans - statistics & numerical data | Male | Indians, North American - statistics & numerical data | Adult | Female | HIV Infections - mortality | Acquired Immunodeficiency Syndrome - ethnology | Risk Assessment | Risk Factors | European Continental Ancestry Group - statistics & numerical data | Logistic Models | African Americans - statistics & numerical data | Adolescent | Survival Analysis | Acquired Immunodeficiency Syndrome - epidemiology | Acquired Immunodeficiency Syndrome - mortality | Aged | HIV Infections - ethnology | Population Surveillance | HIV infection | Ethnicity | Acquired immune deficiency syndrome--AIDS | Human immunodeficiency virus--HIV | Race | Hemophilia | Infections | Regression analysis | Behavior | Drug resistance | Minority & ethnic groups | Drug use | Risk factors | Research and Practice
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30. Full Text Hemophilia growth and development study: Design, methods and entry data
by Hilgartner, Margaret W and Hilgartner, M.W and Donfield, S.M and Donfield, Sharyne M and Willoughby, A and Willoughby, Anne and Contant, Charles F and Contant, C.F and Evatt, B.L and Evatt, Bruce L and Gomperts, E.D and Gomperts, Edward D and Hoots, W.K and Hoots, W. Keith and Jason, Janine and Jason, J and Loveland, Katherine A and Loveland, K.A and McKinlay, Sonja M and McKinlay, S.M and Stehbens, James A and Stehbens, J.A
Journal of Pediatric Hematology/Oncology, ISSN 0192-8562, 1993, Volume 15, Issue 2, pp. 208 - 218
Purpose: The study design, research questions, and baseline data are presented from a multicenter longitudinal epidemiologic investigation of the impact of... 
Neuropsychological functioning | Sexual maturation | Immune function | Hemophilia | Human immunodeficiency virus | Physical growth | Neurologic functioning | K MA HEMATOLOGY | VIRUS-INFECTION | PHYSICAL GROWTH | AIDS | NEUROLOGIC FUNCTIONING | IMMUNE-DEFICIENCY SYNDROME | HEMOPHILIA | ACQUIRED IMMUNODEFICIENCY SYNDROME | CHILDREN | HUMAN IMMUNODEFICIENCY VIRUS | K DM ONCOLOGY | NEUROPSYCHOLOGICAL FUNCTIONING | ONCOLOGY | PEDIATRICS | K TQ PEDIATRICS | IMMUNE FUNCTION | HEMATOLOGY | SEXUAL MATURATION | Age Factors | HIV Seropositivity - complications | Growth Disorders - immunology | Hemophilia A - ethnology | Hemophilia A - immunology | Humans | Growth Disorders - etiology | Male | Sexual Maturation - physiology | Growth Disorders - ethnology | Hemophilia A - complications | Transfusion Reaction | HIV Infections - immunology | HIV Infections - etiology | Adolescent | Adult | Female | Neuropsychology | Continental Population Groups | HIV Infections - ethnology | Child | HIV Seropositivity - immunology | Longitudinal Studies
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31. Full Text Predictors of non‐adherence to prescribed prophylactic clotting‐factor treatment regimens among adolescent and young adults with a bleeding disorder
by Witkop, M. L and McLaughlin, J. M and Anderson, T. L and Munn, J. E and Lambing, A and Tortella, B
Haemophilia, ISSN 1351-8216, 07/2016, Volume 22, Issue 4, pp. e245 - e250
Introduction Adherence to clotting‐factor treatment regimens, especially among adolescents and young adults (AYAs), is under‐researched. Aim We determined... 
predictors | young adult | prophylaxis/prophylactic | adolescents | adherence | Adherence | Prophylaxis/prophylactic | Adolescents | Young adult | Predictors | MODERATE | WELL | BARRIERS | IMPACT | SEVERE HEMOPHILIA | THERAPY | DISEASE | HEMATOLOGY | BENEFITS | Severity of Illness Index | Medication Adherence - ethnology | Humans | European Continental Ancestry Group | Logistic Models | Male | Hemophilia A - pathology | Hemophilia B - drug therapy | Young Adult | Hemophilia B - pathology | Adolescent | Blood Coagulation Factors - therapeutic use | von Willebrand Diseases - drug therapy | Quality of Life | Adult | Female | Surveys and Questionnaires | von Willebrand Diseases - pathology | Internet | Hemophilia A - drug therapy | Odds Ratio | Antibodies, Neutralizing - blood | Insurance, Health | Health care industry | Youth | Teenagers | Patient compliance | Analysis | Hemophilia
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32. Full Text A common ancestral mutation (C128X) occurring in 11 non‐Jewish families from the UK with factor XI deficiency
by Bolton‐Maggs, P. H. B and Peretz, H and Butler, R and Mountford, R and Keeney, S and Zacharski, L and Zivelin, A and Seligsohn, U
Journal of Thrombosis and Haemostasis, ISSN 1538-7933, 06/2004, Volume 2, Issue 6, pp. 918 - 924
Factor XI (FXI) deficiency is a mild bleeding disorder that is particularly common in Ashkenazi Jews, but has been reported in all populations. In Jews, two... 
founder effect | gene mutation | factor XI | Founder effect | Factor XI | Gene mutation | FOUNDERS | GENE | HEMOPHILIA-B | ASHKENAZI JEWS | PERIPHERAL VASCULAR DISEASE | FACTOR-VII DEFICIENCY | HEMATOLOGY | Haplotypes | European Continental Ancestry Group - genetics | Exons | Humans | Middle Aged | Genotype | Male | Codon, Nonsense | Factor XI Deficiency - ethnology | United Kingdom - ethnology | Founder Effect | Molecular Epidemiology | DNA Mutational Analysis | Pedigree | Adolescent | Aged, 80 and over | Adult | Female | Aged | Factor XI Deficiency - genetics | United Kingdom - epidemiology
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33. Full Text Subtype classification of Iranian HIV-1 sequences registered in the HIV databases, 2006-2013
by Baesi, Kazem and Moallemi, Samaneh and Farrokhi, Molood and Alinaghi, Seyed Ahmad Seyed and Truong, Hong-Ha M
PLoS ONE, ISSN 1932-6203, 09/2014, Volume 9, Issue 9, p. e105098
Background: The rate of human immunodeficiency virus type 1 (HIV-1) infection in Iran has increased dramatically in the past few years. While the earliest... 
AFGHANISTAN | TYPE-1 SUBTYPE | MULTIDISCIPLINARY SCIENCES | RESISTANCE | SURVEILLANCE | INJECTING DRUG-USERS | DIVERSITY | INFECTION | EPIDEMIC | GAG | CRF35-AD | Genome, Viral | HIV Infections - epidemiology | HIV Infections - virology | Humans | Afghanistan - ethnology | Molecular Sequence Data | Male | Phylogeny | HIV-1 - genetics | HIV-1 - classification | Hemophilia A - complications | Molecular Epidemiology | Genes, env | Genes, gag | Genes, pol | Female | HIV Infections - transmission | Iran - epidemiology | Substance Abuse, Intravenous - complications | Databases, Nucleic Acid | Infection | Databases | Drug traffic | Analysis | Genomics | Hemophilia | Genomes | HIV (Viruses) | Health aspects | HIV infection | Drug dealing | Epidemics | Drug abuse | Trafficking | Viruses | Infections | Drug resistance | Epidemiology | Data bases | Gene sequencing | Studies | Disease transmission | Gag protein | Acquired immune deficiency syndrome--AIDS | Human immunodeficiency virus--HIV | Phylogenetics | Immigration | AIDS | HIV | Acquired immune deficiency syndrome | Human immunodeficiency virus
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34. Full Text Radionuclide synovectomy and chronic haemophilic synovitis in Asians: a retrospective study
by Chew, E. M. D and Tien, S. L and Sundram, F. X and Ho, Y. K. L and Howe, T. S
Haemophilia, ISSN 1351-8216, 09/2003, Volume 9, Issue 5, pp. 632 - 637
Radionuclide synovectomy has been identified as the procedure of choice in treating chronic haemophilic synovitis among Caucasian populations. Its... 
haemophilia | haemarthrosis | 32P chromic phosphate | quality of life | 188Re–tin colloid | Haemophila | Haemarthrosis | P chromic phosphate | Re-tin colloid | Quality of life | KNEE | ARTHROSCOPIC SYNOVECTOMY | GOLD | P-32 chromic phosphate | MANAGEMENT | ARTHROPATHY | HEMARTHROSIS | FOLLOW-UP | SYNOVIORTHESIS | Re-188-tin colloid | RADIATION SYNOVECTOMY | HEMATOLOGY | Singapore | Follow-Up Studies | Humans | Middle Aged | Male | Patient Satisfaction | Synovitis - etiology | Adult | Synovitis - radiotherapy | Retrospective Studies | Severity of Illness Index | Radioisotopes - therapeutic use | Hemophilia A - ethnology | Treatment Outcome | Hemophilia A - complications | Hemophilia B - complications | Synovial Membrane - radiation effects | Adolescent | Quality of Life | Rhenium - therapeutic use | Hemarthrosis - prevention & control | Hemophilia B - ethnology | Pain Measurement | Phosphorus Radioisotopes - therapeutic use | Chronic Disease
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35. Full Text Maternal low-level somatic mosaicism of Cys155Tyr of F9 in severe hemophilia B
by Kim, Hee-Jung and Lee, Ki-O and Yoo, Ki-Young and Kim, Sun-Hee and Kim, Hee-Jin
Blood Coagulation & Fibrinolysis, ISSN 0957-5235, 12/2015, Volume 26, Issue 8, pp. 866 - 868
Hemophilia B is an X-linked bleeding disorder caused by deficient coagulation factor IX from a mutation in the F9 gene. Here, we report a family with two... 
Hemophilia B | Somatic mosaicism | Mutation | mutation | TRANSMISSION | GENE | hemophilia B | somatic mosaicism | MUTATIONS | HEMATOLOGY | DEFICIENCY | Gene Expression | Humans | Child, Preschool | Molecular Sequence Data | Factor IX - genetics | Male | Hemophilia B - genetics | Mutation, Missense | Genetic Counseling | Sequence Analysis, DNA | Hemizygote | Homozygote | Asian Continental Ancestry Group | Hemophilia B - pathology | Pedigree | Base Sequence | Alleles | Female | Mosaicism | Hemophilia B - ethnology | Amino Acid Substitution | Siblings
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36. Full Text Hermansky–Pudlak syndrome: infrequent bleeding and first report of Turkish and Pakistani kindreds
by Harrison, C and Khair, K and Baxter, B and Russell-Eggitt, I and Hann, I and Liesner, R
Archives of Disease in Childhood, ISSN 0003-9888, 04/2002, Volume 86, Issue 4, pp. 297 - 301
Hermansky–Pudlak syndrome (HPS) is a rare disorder characterised by oculocutaneous albinism, a bleeding tendency, and lipofuscinosis. This retrospective study... 
PEDIATRICS | DEFECTS | PALE EAR EP | GENE | MUTATION | Hermanski-Pudlak Syndrome - ethnology | Pakistan - ethnology | Humans | Male | Turkey - ethnology | Hemorrhagic Disorders - genetics | Hermanski-Pudlak Syndrome - genetics | Pedigree | Hermanski-Pudlak Syndrome - physiopathology | Female | Hemorrhagic Disorders - ethnology | Bleeding Time | Child | Platelet Aggregation - genetics | Albinism | Causes of | Hemorrhage | Hematology | Laboratories | Families & family life | Family medical history | Patients | Molecular weight | Children & youth | Defects | Inflammatory bowel disease | Genotype & phenotype | Pulmonary fibrosis | Blood platelets | Hemophilia | Mutation | Original
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37. Full Text Influence of single nucleotide polymorphisms in factor VIII and von Willebrand factor genes on plasma factor VIII activity: The ARIC Study
by Campos, Marco and Buchanan, Ashley and Yu, Fuli and Barbalic, Maja and Xiao, Yang and Chambless, Lloyd E and Wu, Kenneth K and Folsom, Aaron R and Boerwinkle, Eric and Dong, Jing-Fei
Blood, ISSN 0006-4971, 02/2012, Volume 119, Issue 8, pp. 1929 - 1934
Factor VIII (FVIII) functions as a cofactor for factor IXa in the contact coagulation pathway and circulates in a protective complex with von Willebrand factor... 
LOCALIZATION | POPULATION | VONWILLEBRAND-FACTOR | RISK-FACTORS | ABO LOCUS | HEMOPHILIA-A | LIGHT-CHAIN | DISEASE | BINDING DOMAIN | ATHEROSCLEROSIS | HEMATOLOGY | Haplotypes | European Continental Ancestry Group - genetics | Introns - genetics | Prospective Studies | Risk Assessment | Atherosclerosis - genetics | Gene Frequency | Humans | Middle Aged | Risk Factors | African Americans - genetics | Factor VIII - genetics | Genotype | Male | Atherosclerosis - ethnology | von Willebrand Factor - genetics | Linkage Disequilibrium | Atherosclerosis - blood | Base Sequence | Sex Factors | Female | Polymorphism, Single Nucleotide | Factor VIII - metabolism | Thrombosis and Hemostasis
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38. Full Text Sexuality and haemophilia: connections across the life‐span
by Parish, K. L
Haemophilia, ISSN 1351-8216, 05/2002, Volume 8, Issue 3, pp. 353 - 359
A broad overview of sexuality issues and needs as they relate to haemophilia are presented. Venturing well beyond ‘safer sex’, sexuality is defined here to... 
counselling | haemophilia | sexuality | provider | comprehensive care | Comprehensive care | Haemophilia | Counselling | Sexuality | Provider | HIV | MEN | SAFER SEX | ILLNESS | HEMATOLOGY | HEMOPHILIA | Comprehensive Health Care | Hemophilia A - ethnology | Humans | Sex Counseling | Quality of Life | Hemophilia A - psychology
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39. Full Text Cross‐cultural validation of the CHO‐KLAT and HAEMO‐QoL‐A in Canadian French
by YOUNG, N. L and ST‐LOUIS, J and BURKE, T and HERSHON, L and BLANCHETTE, V
Haemophilia, ISSN 1351-8216, 05/2012, Volume 18, Issue 3, pp. 353 - 357
Multi‐site studies are necessary in the field of haemophilia to ensure adequate sample sizes. Quality of life (QoL) instruments need to be harmonized across... 
haemophilia | quality of life | patient reported outcomes | measurement | validation | Measurement | Validation | Haemophilia | Patient reported outcomes | Quality of life | ADULTS | RELIABILITY | HEMOPHILIA | SF-36 | BOYS | QUALITY-OF-LIFE | OUTCOMES | HEMATOLOGY | NORMATIVE DATA | HEALTH-STATUS | Outcome Assessment (Health Care) - methods | France - ethnology | Reproducibility of Results | Humans | Child, Preschool | Hemophilia B - psychology | Male | Hemophilia A - psychology | Canada | Cross-Cultural Comparison | Language | Quality of Life | Adult | Aged | Child | Surveys and Questionnaires - standards | Translations
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40. Full Text The prevalence of factor VIII inhibitors and genetic aspects of inhibitor development in Chinese patients with haemophilia A
by WANG, X. F and ZHAO, Y. Q and YANG, R. C and WU, J. S and SUN, J and ZHANG, X. S and DING, Q. L and GE, H. L and WANG, H. L
Haemophilia, ISSN 1351-8216, 07/2010, Volume 16, Issue 4, pp. 632 - 639
The prevalence of inhibitors in Chinese haemophiliacs has not yet been reported. The aim of this study was to identify the prevalence of factor VIII (FVIII)... 
Chinese | haemophilia A | inhibitor | factor VIII | genotype | Genotype | Haemophilia A |