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medical and health sciences (31) 31
medicin och hälsovetenskap (31) 31
clinical medicine (30) 30
klinisk medicin (30) 30
hematology (23) 23
humans (21) 21
hematologi (20) 20
index medicus (16) 16
female (15) 15
male (15) 15
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child (11) 11
infant (11) 11
children (10) 10
pediatrik (10) 10
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adolescent (7) 7
adult (7) 7
mutation (7) 7
risk factors (5) 5
thrombocytopenia (5) 5
childhood (4) 4
factor viii (4) 4
heterozygote (4) 4
incidence (4) 4
middle aged (4) 4
pedigree (4) 4
prenatal diagnosis (4) 4
prospective studies (4) 4
scandinavian and nordic countries - epidemiology (4) 4
abridged index medicus (3) 3
analysis (3) 3
anemia (3) 3
article (3) 3
asparaginase - adverse effects (3) 3
basic medicine (3) 3
epidemiology (3) 3
genetic predisposition to disease (3) 3
hemophilia (3) 3
hemophilia a (3) 3
hemophilia a - genetics (3) 3
infant, newborn (3) 3
management (3) 3
medicinska och farmaceutiska grundvetenskaper (3) 3
myelodysplastic syndromes (3) 3
pregnancy (3) 3
purpura, thrombocytopenic, idiopathic - epidemiology (3) 3
research (3) 3
risk (3) 3
time factors (3) 3
treatment outcome (3) 3
young adult (3) 3
acute myeloid-leukemia (2) 2
age factors (2) 2
alleles (2) 2
amniocentesis (2) 2
antibodies - blood (2) 2
anticoagulants (2) 2
anticoagulants - adverse effects (2) 2
antineoplastic agents - adverse effects (2) 2
antineoplastic combined chemotherapy protocols - adverse effects (2) 2
antineoplastic combined chemotherapy protocols - therapeutic use (2) 2
asparaginase (2) 2
ataxia (2) 2
cancer (2) 2
carriers (2) 2
chronic disease (2) 2
coagulation (2) 2
congenital dyserythropoietic anaemia (2) 2
drug therapy (2) 2
experience (2) 2
factor ix (2) 2
factor viii - immunology (2) 2
factor viii - therapeutic use (2) 2
fanconi-anemia (2) 2
finland - epidemiology (2) 2
follow-up (2) 2
follow-up studies (2) 2
gender (2) 2
gene mutations (2) 2
genetic association studies (2) 2
genotype (2) 2
germ-line (2) 2
haemophilia a (2) 2
haemophilia b (2) 2
haemorrhage (2) 2
health aspects (2) 2
hemophilia a - drug therapy (2) 2
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hemophilia prenatal diagnosis. genetic counseling. hemophilia a hemophilia b prenatal diagnosis. genetic counseling (2) 2
hemorrhage (2) 2
hemorrhage - epidemiology (2) 2
homozygote (2) 2
infant mental health (2) 2
inherited anaemia (2) 2
inhibitors (2) 2
interleukin 1 receptor antagonist protein - genetics (2) 2
itp (2) 2
journal article (2) 2
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1. Full Text An Autoinflammatory Disease with Deficiency of the Interleukin-1–Receptor Antagonist
by Aksentijevich, Ivona and Masters, Seth L and Ferguson, Polly J and Dancey, Paul and Frenkel, Joost and van Royen-Kerkhoff, Annet and Laxer, Ron and Tedgård, Ulf and Cowen, Edward W and Pham, Tuyet-Hang and Booty, Matthew and Estes, Jacob D and Sandler, Netanya G and Plass, Nicole and Stone, Deborah L and Turner, Maria L and Hill, Suvimol and Butman, John A and Schneider, Rayfel and Babyn, Paul and El-Shanti, Hatem I and Pope, Elena and Barron, Karyl and Bing, Xinyu and Laurence, Arian and Lee, Chyi-Chia R and Chapelle, Dawn and Clarke, Gillian I and Ohson, Kamal and Nicholson, Marc and Gadina, Massimo and Yang, Barbara and Korman, Benjamin D and Gregersen, Peter K and van Hagen, P. Martin and Hak, A. Elisabeth and Huizing, Marjan and Rahman, Proton and Douek, Daniel C and Remmers, Elaine F and Kastner, Daniel L and Goldbach-Mansky, Raphaela and Paediatric Hematologic Research Group and Enheten för pediatrisk hematologi and Lund University and Lunds universitet
The New England Journal of Medicine, ISSN 0028-4793, 06/2009, Volume 360, Issue 23, pp. 2426 - 2437
In nine patients with neonatal onset of severe inflammatory lesions affecting mainly bone and skin and associated with mutations of IL1RN, which encodes the... 
CELLS | MEDICINE, GENERAL & INTERNAL | GENE-CLUSTER | INFLAMMASOME | MUTATIONS | CIAS1 | SECRETION | ARTHRITIS | ASSOCIATION | INFANTILE CORTICAL HYPEROSTOSIS | FAMILY | Interleukin-1 - genetics | Humans | Infant | Interleukin 1 Receptor Antagonist Protein - genetics | Male | RNA, Messenger - metabolism | Autoimmune Diseases - genetics | Inflammation - drug therapy | Base Sequence | Interleukin-1 - physiology | Female | Child | Autoimmune Diseases - drug therapy | Infant, Newborn | Interleukin 1 Receptor Antagonist Protein - deficiency | Interleukin-1beta - antagonists & inhibitors | Inflammation - immunology | Genes, Recessive | Homozygote | Interleukin 1 Receptor Antagonist Protein - therapeutic use | Anti-Inflammatory Agents, Non-Steroidal - therapeutic use | Pedigree | Inflammation - genetics | Mutation | Receptors, Interleukin-1 - antagonists & inhibitors | Interleukin-1 | Usage | Gene mutations | Causes of | Research | Autoimmune diseases | Drug therapy | Health aspects | Proteins | Genetics | Skin | Genetic testing | Clinical Medicine | Pediatrics | Medical and Health Sciences | Hematologi | Hematology | Medicin och hälsovetenskap | Pediatrik | Klinisk medicin
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2. Full Text SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies
by Davidsson, Josef and Puschmann, Andreas and Tedgård, Ulf and Bryder, David and Nilsson, Lars and Cammenga, Jörg and Medicinska fakulteten and Region Östergötland and Linköpings universitet and Institutionen för klinisk och experimentell medicin and Centrum för kirurgi, ortopedi och cancervård and Avdelningen för Kirurgi, Ortopedi och Onkologi and Hematologiska kliniken US
Leukemia, ISSN 0887-6924, 05/2018, Volume 32, Issue 5, pp. 1106 - 1115
Germline mutations in the SAMD9 and SAMD9L genes, located in tandem on chromosome 7, are associated with a clinical spectrum of disorders including the MIRAGE... 
C-MONOSOMY | HEMATOPOIESIS | ONCOLOGY | CEREBELLAR-ATAXIA | DISORDER | CHROMOSOME-7 | HYPOPLASTIC-ANEMIA | LEUKEMIA | HEMATOLOGY | MYELODYSPLASTIC SYNDROME | FANCONI-ANEMIA | SOMATIC MUTATIONS | Proteins - genetics | Genetic Predisposition to Disease | Humans | Tumor Suppressor Proteins - genetics | Germ-Line Mutation | Heterozygote | Myelodysplastic Syndromes - genetics | Ataxia - genetics | Pancytopenia - genetics | Leukemia, Myeloid, Acute - genetics | Care and treatment | Genetic aspects | Research | Gene mutations | Chromosomes | Myelodysplastic syndromes | Cerebellum | Adrenal glands | Leukemia | Glands | Myelodysplasia | Hemorrhage | Myelodysplastic syndrome | Thymus | Atrophy | Ataxia | Children | Monosomy | Hypoplasia | Phenotypes | Hematology | Anemia | Blood cells | Chromosome 7 | Ovaries | Patients | Hemopoiesis | Carriers | Pancytopenia | Nystagmus | Mutation | Testes | Cancer genetics | Genetics research | Review | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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3. Full Text Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms
by Tesi, Bianca and Davidsson, Josef and Voss, Matthias and Rahikkala, Elisa and Holmes, Tim D and Chiang, Samuel C. C and Komulainen-Ebrahim, Jonna and Gorcenco, Sorina and Nilsson, Alexandra Rundberg and Ripperger, Tim and Kokkonen, Hannaleena and Bryder, David and Fioretos, Thoas and Henter, Jan-Inge and Möttönen, Merja and Niinimäki, Riitta and Nilsson, Lars and Pronk, Cornelis Jan and Puschmann, Andreas and Qian, Hong and Uusimaa, Johanna and Moilanen, Jukka and Tedgård, Ulf and Cammenga, Jörg and Bryceson, Yenan T and Medicinska fakulteten and Region Östergötland and Linköpings universitet and Institutionen för klinisk och experimentell medicin and Centrum för kirurgi, ortopedi och cancervård and Avdelningen för Kirurgi, Ortopedi och Onkologi and Hematologiska kliniken US
Blood, ISSN 0006-4971, 04/2017, Volume 129, Issue 16, pp. 2266 - 2279
Several monogenic causes of familial myelodysplastic syndrome (MDS) have recently been identified. We studied 2 families with cytopenia, predisposition to MDS... 
FAMILIAL TUMORAL CALCINOSIS | GERM-LINE | FANCONI-ANEMIA REGISTRY | HEMATOPOIETIC STEM-CELLS | IN-VIVO | SPONTANEOUS REMISSION | ACUTE MYELOID-LEUKEMIA | RETROSPECTIVE ANALYSIS | HEMATOLOGY | DETECTABLE CLONAL MOSAICISM | MYELODYSPLASTIC SYNDROMES | Cell Proliferation | Humans | Middle Aged | Pancytopenia - immunology | Male | Killer Cells, Natural - pathology | Cognitive Dysfunction - immunology | Interferon Type I - pharmacology | Myeloid Cells - immunology | Tumor Suppressor Proteins - genetics | Killer Cells, Natural - immunology | Adult | Cognitive Dysfunction - genetics | Female | Myeloid Cells - drug effects | Cognitive Dysfunction - diagnosis | B-Lymphocytes - pathology | Cognitive Dysfunction - complications | Immunologic Deficiency Syndromes - diagnosis | Immunologic Deficiency Syndromes - immunology | Child | Gene Expression | Tumor Suppressor Proteins - metabolism | Immunologic Deficiency Syndromes - complications | Pancytopenia - diagnosis | Immunophenotyping | Myelodysplastic Syndromes - complications | B-Lymphocytes - drug effects | Hematopoiesis - immunology | Myelodysplastic Syndromes - diagnosis | B-Lymphocytes - immunology | Pancytopenia - complications | Pedigree | Alleles | Immunologic Deficiency Syndromes - genetics | Heterozygote | Mosaicism | Killer Cells, Natural - drug effects | Myelodysplastic Syndromes - genetics | Mutation | Myeloid Cells - pathology | Chromosomes, Human, Pair 7 - chemistry | Pancytopenia - genetics | Myelodysplastic Syndromes - immunology | Myeloid Neoplasia | Clinical Medicine | Medical and Health Sciences | Hematology | Hematologi | Klinisk medicin | Medicin och hälsovetenskap
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4. Full Text Thromboembolism in acute lymphoblastic leukemia: Results of nopho all2008 protocol treatment in patients aged 1 to 45 years
by Rank, Cecilie Utke and Toft, Nina and Tuckuviene, Ruta and Grell, Kathrine and Nielsen, Ove Juul and Frandsen, Thomas Leth and Marquart, Hanne Vibeke Hansen and Albertsen, Birgitte Klug and Tedgård, Ulf and Hallböök, Helene and Ruud, Ellen and Jarvis, Kirsten Brunsvig and Quist-Paulsen, Petter and Huttunen, Pasi and Wartiovaara-Kautto, Ulla and Jónsson, Ólafur Gísli and Trakymiene, Sonata Saulyte and Griškevičius, Laimonas and Saks, Kadri and Punab, Mari and Schmiegelow, Kjeld and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Uppsala universitet and Institutionen för medicinska vetenskaper and Hematologi
Blood, ISSN 0006-4971, 05/2018, Volume 131, Issue 22, pp. 2475 - 2484
Thromboembolism frequently occurs during acute lymphoblastic leukemia (ALL) therapy. We prospectively registered thromboembolic events during the treatment of... 
L-ASPARAGINASE | ADULT PATIENTS | THROMBOTIC COMPLICATIONS | RISK-FACTORS | VENOUS THROMBOEMBOLISM | INDUCTION THERAPY | ANTITHROMBIN | COAGULATION | HEMATOLOGY | CHEMOTHERAPY | CHILDREN | Precursor Cell Lymphoblastic Leukemia-Lymphoma - complications | Age Factors | Thromboembolism - chemically induced | Humans | Middle Aged | Risk Factors | Antineoplastic Combined Chemotherapy Protocols - adverse effects | Child, Preschool | Infant | Male | Antineoplastic Agents - therapeutic use | Incidence | Young Adult | Asparaginase - adverse effects | Thromboembolism - prevention & control | Antineoplastic Agents - adverse effects | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Adolescent | Adult | Female | Asparaginase - therapeutic use | Child | Lymphoid Neoplasia | Clinical Medicine | Medical and Health Sciences | Hematology | Hematologi | Klinisk medicin | Medicin och hälsovetenskap
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5. Full Text A novel 33‐Gene targeted resequencing panel provides accurate, clinical‐grade diagnosis and improves patient management for rare inherited anaemias
by Roy, Noémi B. A and Wilson, Edward A and Henderson, Shirley and Wray, Katherine and Babbs, Christian and Okoli, Steven and Atoyebi, Wale and Mixon, Avery and Cahill, Mary R and Carey, Peter and Cullis, Jonathan and Curtin, Julie and Dreau, Helene and Ferguson, David J. P and Gibson, Brenda and Hall, Georgina and Mason, Joanne and Morgan, Mary and Proven, Melanie and Qureshi, Amrana and Sanchez Garcia, Joaquin and Sirachainan, Nongnuch and Teo, Juliana and Tedgård, Ulf and Higgs, Doug and Roberts, David and Roberts, Irene and Schuh, Anna
British Journal of Haematology, ISSN 0007-1048, 10/2016, Volume 175, Issue 2, pp. 318 - 330
Summary Accurate diagnosis of rare inherited anaemias is challenging, requiring a series of complex and expensive laboratory tests. Targeted... 
molecular genetics | inherited anaemia | congenital dyserythropoietic anaemia | pyruvate kinase deficiency | next‐generation sequencing | VARIANTS | next-generation sequencing | STANDARDS | DEFICIENCY | PRECISION | HEMOLYTIC-ANEMIA | DIAMOND-BLACKFAN ANEMIA | MUTATIONS | HEMATOLOGY | WHOLE GENOME | BONE-MARROW FAILURE | REVEALS | Computational Biology - methods | Genetic Predisposition to Disease | Reproducibility of Results | Genetic Association Studies | Genetic Testing - standards | Humans | Anemia - diagnosis | Infant | Male | Workflow | Rare Diseases | Genetic Testing - methods | Anemia - genetics | Disease Management | High-Throughput Nucleotide Sequencing | Polymorphism, Single Nucleotide | Mutation | Genetic disorders | Diagnostic equipment (Medical) | Molecular genetics | Anemia | Genes | Diagnosis | Nucleotide sequencing | DNA sequencing | Red Cells and Iron | Research Paper | Clinical Medicine | Congenital dyserythropoietic anaemia | Next-generation sequencing | Inherited anaemia | Hematologi | Medical and Health Sciences | Hematology | Medicin och hälsovetenskap | Pyruvate kinase deficiency | Klinisk medicin
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6. Full Text Cerebral sinus venous thromboses in children with acute lymphoblastic leukaemia – a multicentre study from the Nordic Society of Paediatric Haematology and Oncology
by Ranta, Susanna and Tuckuviene, Ruta and Mäkipernaa, Anne and Albertsen, Birgitte K and Frisk, Tony and Tedgård, Ulf and Jónsson, Ólafur G and Pruunsild, Kaie and Gretenkort Andersson, Nadine and Winther Gunnes, Maria and Saulyte Trakymiene, Sonata and Frandsen, Thomas and Heyman, Mats and Ruud, Ellen and Helgestad, Jon and Paediatric Hematologic Research Group and Enheten för pediatrisk hematologi and Lund University and Lunds universitet
British Journal of Haematology, ISSN 0007-1048, 02/2015, Volume 168, Issue 4, pp. 547 - 552
Summary We present a prospective multicentre cohort of 20 children with acute lymphoblastic leukaemia (ALL) and cerebral sinus venous thrombosis (CSVT). The... 
cerebral sinovenous thrombosis | acute leukaemia | paediatric | ASPARAGINASE | METAANALYSIS | SINOVENOUS THROMBOSIS | PROTOCOL | RISK | HEMATOLOGY | ISCHEMIC-STROKE | CANCER | Baltic States - epidemiology | Prospective Studies | Humans | Antineoplastic Combined Chemotherapy Protocols - adverse effects | Child, Preschool | Infant | Male | Consolidation Chemotherapy | Sinus Thrombosis, Intracranial - epidemiology | Incidence | Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy | Asparaginase - adverse effects | Female | Child | Scandinavian and Nordic Countries - epidemiology | Precursor Cell Lymphoblastic Leukemia-Lymphoma - complications | Risk Factors | Sinus Thrombosis, Intracranial - etiology | Anticoagulants - therapeutic use | Treatment Outcome | Anticoagulants - adverse effects | Asparaginase - administration & dosage | Adrenal Cortex Hormones - adverse effects | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Adolescent | Sinus Thrombosis, Intracranial - drug therapy | Paediatric | Acute leukaemia | Cerebral sinovenous thrombosis | Pediatrics | Trade and professional associations | Children | Clinical Medicine | Hematologi | Medical and Health Sciences | Hematology | Medicin och hälsovetenskap | Klinisk medicin
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7. Full Text Lupus anticoagulants in two children—bleeding due to nonphospholipid-dependent antiprothrombin antibodies
by Knobe, Karin and Tedgård, Ulf and Ek, Torben and Sandström, Per-Erik and Hillarp, Andreas and Medicinska fakulteten and Institutionen för klinisk vetenskap and Pediatrik and Umeå universitet
European Journal of Pediatrics, ISSN 0340-6199, 9/2012, Volume 171, Issue 9, pp. 1383 - 1387
We describe two children with significant bleeding: one with multiple ecchymoses and the other with scrotal bleeding. In both patients, the activated partial... 
Pediatrics | Lupus anticoagulants | Medicine & Public Health | Coagulation | Antiprothrombin antibodies | Children | Bleeding | MECHANISM | THROMBOSIS | IDIOPATHIC CEREBRAL-ISCHEMIA | IGG | PREVALENCE | ANTIPHOSPHOLIPID SYNDROME | ACQUIRED HYPOPROTHROMBINEMIA | PEDIATRICS | INHIBITORS | ANTI-PROTHROMBIN ANTIBODIES | Lupus Coagulation Inhibitor - blood | Humans | Prothrombin Time | Child, Preschool | Male | Biomarkers - blood | Blood Coagulation Disorders - virology | Partial Thromboplastin Time | Adenoviridae Infections - complications | Blood Coagulation Disorders - blood | Female | Hemorrhagic Disorders - etiology | Blood Coagulation Disorders - diagnosis | Prothrombin - metabolism | Child | Blood Coagulation Disorders - complications | Lupus | Viral antibodies | Medical examination | Prothrombin | Antibodies | Thrombin | Anticoagulants (Medicine) | Blood | Clinical Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Pediatrik | Klinisk medicin
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8. Full Text Establishing a regional paediatric registry improved the overview and detection of side effects in children on anticoagulants
by Jeremiasen, Ida and Hanséus, Katarina and Naumann, Pernilla and Nilsson, Camilla and Tedgård, Ulf and Svensson, Peter J and Andersson, Nadine G and Children cardiology and Paediatrics (Lund) and Lund University and Paediatric Haematology Research Unit and Pediatrisk hematologi and Pediatrik, Lund and Barnkardiologi and Paediatric Hematologic Research Group and Enheten för pediatrisk hematologi and Lunds universitet
Acta Paediatrica, ISSN 0803-5253, 01/2018, Volume 107, Issue 1, pp. 166 - 167
PEDIATRICS | Complications and side effects | Pediatrics | Anticoagulants (Medicine) | Anticoagulants | Side effects | Children | Clinical Medicine | Hematologi | Medical and Health Sciences | Hematology | Medicin och hälsovetenskap | Pediatrik | Klinisk medicin
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9. Full Text Parenting stress and its correlates in an infant mental health unit : a cross-sectional study
by Tedgård, Eva and Tedgård, Ulf and Råstam, Maria and Johansson, Björn Axel and Utvecklingsrelaterade störningar, affektiv sjukdom och ångestsyndrom i barn- och ungdomspsykiatri and Lund University and Paediatric Haematology Research Unit and Pediatrisk hematologi and Disorders in clinical child and adolescent psychiatry and Lunds universitet
Nordic Journal of Psychiatry, ISSN 0803-9488, 09/2019
Background: An infant’s development is closely linked to the relationship they have with their parents. Parenting stress, affective disorder, and an upbringing... 
parenting stress | Clinical Medicine | Pediatrics | gender | Medical and Health Sciences | Medicin och hälsovetenskap | Pediatrik | Infant mental health | Psykiatri | postnatal affective disorder | Klinisk medicin | Psychiatry
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10. Full Text Breath‐holding spells occur disproportionately more often in children with transient erythroblastopenia
by Hellström Schmidt, Sanna and Tedgård, Ulf and Pronk, Cornelis J.H and Division of Molecular Hematology (DMH) and Avdelningen för molekylär hematologi and Lund University and Paediatric Haematology Research Unit and Pediatrisk hematologi and Paediatric Hematologic Research Group and Enheten för pediatrisk hematologi and Hematopoetisk och immunologisk utveckling and Hematopoietic and immunologic developement and Lunds universitet
Acta Paediatrica, ISSN 0803-5253, 09/2016, Volume 105, Issue 9, pp. 1088 - 1093
Aim This study aimed to evaluate the concomitant occurrence and possible association of breath‐holding spells (BHS) and transient erythroblastopenia of... 
Breath‐holding spells | Paediatric | Transient erythroblastopenia of childhood | Anaemia | Breath-holding spells | ERYTHROPOIESIS | SIBLINGS | PEDIATRICS | CHILDHOOD | Humans | Anemia, Hemolytic, Congenital - blood | Breath Holding | Female | Infant | Male | Anemia, Hemolytic, Congenital - physiopathology | Retrospective Studies | Anemia | Analysis | Children | Health risk assessment | Clinical Medicine | Pediatrics | Hematologi | Medical and Health Sciences | Hematology | Medicin och hälsovetenskap | Pediatrik | Klinisk medicin
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11. Full Text Various regimens for prophylactic treatment of patients with haemophilia
by Schwarz, Rudolf and Ljung, Rolf and Tedgård, Ulf and Paediatrics (Lund) and Lund University and Paediatric Haematology Research Unit and Pediatrisk hematologi and Pediatrik, Lund and Paediatric Hematologic Research Group and Enheten för pediatrisk hematologi and Lunds universitet
European Journal of Haematology, ISSN 0902-4441, 02/2015, Volume 94, Issue 77, pp. 11 - 16
Haemophilia prophylaxis is superior to on‐demand treatment to prevent joint damage. ‘High‐dose prophylaxis’ as used in Sweden is more effective in preventing... 
haemophilia | treatment | inhibitors | children | prophylaxis | Haemophilia | Inhibitors | Treatment | Children | Prophylaxis | CANADIAN HEMOPHILIA | MRI SCALE | ARTHROPATHY | FOLLOW-UP | TAILORED PROPHYLAXIS | JOINT HEALTH SCORE | ON-DEMAND | INHIBITOR DEVELOPMENT | QUALITY-OF-LIFE | FACTOR VIII | HEMATOLOGY | Factor VIII - immunology | Joints - blood supply | Hemophilia A - diagnostic imaging | Age Factors | Humans | Child, Preschool | Infant | Factor VIII - antagonists & inhibitors | Ultrasonography | Arthritis - immunology | Adult | Arthritis - prevention & control | Factor VIII - therapeutic use | Drug Administration Schedule | Arthritis - pathology | Joints - drug effects | Arthritis - diagnostic imaging | Hemophilia A - immunology | Risk Factors | Catheterization, Central Venous | Joints - pathology | Hemophilia A - pathology | Magnetic Resonance Imaging | Joints - immunology | Hemarthrosis - immunology | Hemarthrosis - diagnostic imaging | Quality of Life | Antibodies - blood | Hemarthrosis - pathology | Hemarthrosis - prevention & control | Hemophilia A - drug therapy | Drug therapy | Medicine, Preventive | Hemophilia | Preventive health services | Clinical Medicine | Hematologi | Medical and Health Sciences | Hematology | Medicin och hälsovetenskap | Klinisk medicin
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12. Full Text Duration and morbidity of chronic immune thrombocytopenic purpura in children: five‐year follow‐up of a Nordic cohort
by Rosthøj, Steen and Rajantie, Jukka and Treutiger, Iris and Zeller, Bernward and Tedgård, Ulf and Henter, Jan‐Inge and NOPHO ITP Working Grp and NOPHO ITP Working Group
Acta Paediatrica, ISSN 0803-5253, 07/2012, Volume 101, Issue 7, pp. 761 - 766
Aim:  To describe the clinical course, morbidity and platelet recovery in an unselected Nordic cohort of children with chronic Immune Thrombocytopenic Purpura... 
Thrombocytopenia | Platelets | Chronic ITP | MANAGEMENT | SPONTANEOUS-RECOVERY | CHILDHOOD-ITP | IDIOPATHIC THROMBOCYTOPENIA | ADULTS | PEDIATRICS | SPLENECTOMY | ITP-STUDY-GROUP | INTRACRANIAL HEMORRHAGE | Prognosis | Prospective Studies | Follow-Up Studies | Humans | Child, Preschool | Hospitalization - statistics & numerical data | Infant | Male | Recovery of Function | Purpura, Thrombocytopenic, Idiopathic - blood | Splenectomy | Purpura, Thrombocytopenic, Idiopathic - therapy | Time Factors | Female | Purpura, Thrombocytopenic, Idiopathic - epidemiology | Child | Infant, Newborn | Scandinavian and Nordic Countries - epidemiology | Severity of Illness Index | Kaplan-Meier Estimate | Platelet Count | Adolescent | Remission, Spontaneous | Chronic Disease | Finland - epidemiology | Clinical Medicine | Pediatrics | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Pediatrik
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13. Full Text SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies
by Davidsson, Josef and Puschmann, Andreas and Tedgård, Ulf and Bryder, David and Nilsson, Lars and Cammenga, Jörg and Division of Molecular Hematology (DMH) and Avdelningen för molekylär hematologi and Lund University and Klinisk neurogenetik and Paediatric Haematology Research Unit and StemTherapy: National Initiative on Stem Cells for Regenerative Therapy and MultiPark: Multidisciplinary research focused on Parkinson´s disease and Pediatrisk hematologi and Developmental Hematopoiesis and Utvecklingshematopoes and Clinical Neurogenetics and Lunds universitet
Leukemia, ISSN 0887-6924, 05/2018, Volume 32, Issue 5, p. 1106
Germline mutations in the SAMD9 and SAMD9L genes, located in tandem on chromosome 7, are associated with a clinical spectrum of disorders including the MIRAGE... 
Basic Medicine | SAMD9L | Neurosciences | SAMD9 | Medical and Health Sciences | Medicin och hälsovetenskap | myeloid malignancies | Klinisk medicin | Clinical Medicine | Medicinska och farmaceutiska grundvetenskaper | Ataxia | Cancer and Oncology | Neurovetenskaper | Cancer och onkologi
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14. Full Text Parenting stress and its correlates in an infant mental health unit: a cross-sectional study
by Tedgård, Eva and Tedgård, Ulf and Råstam, Maria and Johansson, Björn Axel and Institute of Neuroscience and Physiology and Gillberg Neuropsychiatry Centre and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy and Sahlgrenska akademin and Institutionen för neurovetenskap och fysiologi
Nordic Journal of Psychiatry, ISSN 0803-9488, 09/2019, pp. 1 - 10
Background: An infant's development is closely linked to the relationship they have with their parents. Parenting stress, affective disorder, and an upbringing... 
parenting stress | Neurosciences | adversity | gender | childhood | maltreatment history | hospital anxiety | postnatal affective disorder | psychological distress | depressive symptoms | alcohol-use disorders | gender-differences | Infant mental health | postpartum | depression | Psychiatry | maternal depression | Neurovetenskaper | intergenerational transmission
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