Articles

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (93) 93
male (66) 66
female (63) 63
index medicus (55) 55
child (54) 54
pediatrics (51) 51
infant (45) 45
child, preschool (39) 39
children (39) 39
adolescent (35) 35
gastroenterology & hepatology (32) 32
prevalence (18) 18
turkey (17) 17
disease (16) 16
mutation (16) 16
treatment outcome (15) 15
turkey - epidemiology (15) 15
medicine & public health (13) 13
diagnosis (12) 12
diagnosis, differential (11) 11
liver (11) 11
nutrition & dietetics (10) 10
oncology (10) 10
case-control studies (9) 9
celiac disease (9) 9
mutations (9) 9
transplantation (9) 9
biopsy (8) 8
childhood (8) 8
diarrhea (8) 8
gastroenterology (8) 8
hematology (8) 8
infant, newborn (8) 8
abridged index medicus (7) 7
article (7) 7
digestive system diseases (7) 7
immunology (7) 7
retrospective studies (7) 7
risk factors (7) 7
universities and colleges (7) 7
adult (6) 6
analysis (6) 6
consanguinity (6) 6
enzyme-linked immunosorbent assay (6) 6
health aspects (6) 6
immunoglobulin a - blood (6) 6
liver - pathology (6) 6
liver diseases (6) 6
liver-transplantation (6) 6
severity of illness index (6) 6
sindirim sistemi hastalıkları (6) 6
animals (5) 5
cirrhosis (5) 5
colitis (5) 5
diet (5) 5
familial mediterranean fever (5) 5
familial mediterranean fever - complications (5) 5
follow-up studies (5) 5
genotype (5) 5
helicobacter pylori (5) 5
hepatology (5) 5
infection (5) 5
inflammatory-bowel-disease (5) 5
liver transplantation - adverse effects (5) 5
management (5) 5
medicine (5) 5
microbiology (5) 5
recurrence (5) 5
rotavirus (5) 5
3-d culture model (4) 4
biomarkers - blood (4) 4
biomedicine (4) 4
breast feeding (4) 4
care and treatment (4) 4
cdd (4) 4
celiac disease - complications (4) 4
celiac disease - epidemiology (4) 4
celiac disease - immunology (4) 4
celiac disease - pathology (4) 4
clinical practice (4) 4
colitis - etiology (4) 4
comorbidity (4) 4
constipation (4) 4
deficiency (4) 4
diabetes (4) 4
encopresis (4) 4
endoscopy (4) 4
endoscopy, gastrointestinal (4) 4
fatal outcome (4) 4
gastrointestinal diseases (4) 4
gastrointestinal hemorrhage - etiology (4) 4
gene (4) 4
genetic aspects (4) 4
genomic (4) 4
guidelines (4) 4
homozygote (4) 4
infants (4) 4
infectious diseases (4) 4
medical colleges (4) 4
medical microbiology (4) 4
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text ACOX2 deficiency
: A disorder of bile acid synthesis with transaminase elevation, liver fibrosis, ataxia, and cognitive impairment
by Sílvia Vilarinho and Sinan Sari and Francesca Mazzacuva and Kaya Bilgüvar and Güldal Esendagli-Yilmaz and Dhanpat Jain and Gülen Akyol and Buket Dalgiç and Murat Günel and Peter T. Clayton and Richard P. Lifton
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2016, Volume 113, Issue 40, pp. 11289 - 11293
( ) encodes branched-chain acyl-CoA oxidase, a peroxisomal enzyme believed to be involved in the metabolism of branched-chain fatty acids and bile acid... 
Branched-chain acyl-CoA oxidase | Idiopathic liver disease | Whole-exome sequencing | Bile acid metabolism | Peroxisomal disorder | DIAGNOSIS | branched-chain acyl-CoA oxidase | MULTIDISCIPLINARY SCIENCES | FAILURE | idiopathic liver disease | ZELLWEGER-SYNDROME | BIOSYNTHESIS | DISEASE | bile acid metabolism | ACYL-COA OXIDASE | MUTATIONS | peroxisomal disorder | whole-exome sequencing | ONSET | Physiological aspects | Ataxia | Biosynthesis | Bile acids | Liver diseases | Health aspects | Biological Sciences
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Mutant neurogenin‐3 in a Turkish boy with congenital malabsorptive diarrhea
by Ünlüsoy Aksu, Aysel and Eğritaş Gürkan, Ödül and Sarı, Sinan and Demirtaş, Zeliha and Türkyılmaz, Canan and Poyraz, Aylar and Dalgıç, Buket
Pediatrics International, ISSN 1328-8067, 05/2016, Volume 58, Issue 5, pp. 379 - 382
Congenital diarrheal disorders are caused by disruption in nutrient digestion, absorption, or transport, enterocyte development and functioning, or... 
cholestyramine | diabetes mellitus | congenital diarrhea | neurogenin‐3 | neurogenin-3 | CELLS | PEDIATRICS | Diarrhea | Genetic disorders | Diabetes | Mutation | Rodents | Electrolyte balance | Nutrient transport | Diabetes mellitus | Differentiation (biology) | Cell differentiation | Neurogenin | Stools | Electrolytic cells | Intestine | Islet cells | Malabsorption | Islets of Langerhans | Pancreas | Acidosis | Metabolic acidosis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text The effect of Helicobacter pylori eradication on functional dyspepsia in Turkish children
by Ünlüsoy Aksu, Aysel and Yılmaz, Güldal and Eğritaş Gürkan, Ödül and Sarı, Sinan and Dalgıç, Buket
Helicobacter, ISSN 1083-4389, 08/2018, Volume 23, Issue 4, pp. e12497 - n/a
Background The aim of this study was to evaluate the effect of Helicobacter pylori (H. pylori) eradication on dyspepsia symptom scores in children with... 
children | Helicobacter pylori eradication | functional dyspepsia | ENDOSCOPY | MANAGEMENT | ABDOMINAL-PAIN | GUIDELINES | MICROBIOLOGY | SYMPTOMS | PREVALENCE | TRIAL | THERAPY | ADOLESCENTS | INFECTION | GASTROENTEROLOGY & HEPATOLOGY | Urea | Helicobacter infections | Children | Helicobacter pylori | Dyspepsia | Antiulcer drugs | Health care | Pathogens | Therapy | Endoscopes | Diagnostic systems | Endoscopy | Patients
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Prevalence of Celiac Disease in Healthy Turkish School Children
by Dalgic, Buket and Sari, Sinan and Basturk, Bilkay and Ensari, Arzu and Egritas, Odul and Bukulmez, Aysegul and Baris, Zeren and Turkish Celiac Study Grp and Turkish Celiac Study Group
The American Journal of Gastroenterology, ISSN 0002-9270, 08/2011, Volume 106, Issue 8, pp. 1512 - 1517
OBJECTIVES: Epidemiological studies of celiac disease (CD) in Turkey have been performed only within some regions of the country. The aim of this study was to... 
DIAGNOSIS | POPULATION | TISSUE TRANSGLUTAMINASE ANTIBODIES | ASSAY | BIOPSY | SENSITIVITY | GASTROENTEROLOGY & HEPATOLOGY | ALWAYS | ADULT | SEROLOGICAL MARKER | ACCURACY | Glutens - immunology | Predictive Value of Tests | Prevalence | Intestine, Small - pathology | Autoantibodies - blood | Humans | Male | Mass Screening - methods | Transglutaminases - immunology | Celiac Disease - immunology | Sensitivity and Specificity | Celiac Disease - complications | Female | Child | Fluorescent Antibody Technique, Indirect | Abdominal Pain - etiology | Biomarkers - blood | Constipation - etiology | Celiac Disease - diagnosis | Celiac Disease - pathology | Turkey - epidemiology | Biopsy | Immunoglobulin A - immunology | Adolescent | Immunoglobulin A - blood | Antibodies - blood | Diarrhea - etiology | Celiac Disease - epidemiology | Intestine, Small - metabolism
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Intestinal Failure and Aberrant Lipid Metabolism in Patients With DGAT1 Deficiency
by van Rijn, Jorik M and Ardy, Rico Chandra and Kuloğlu, Zarife and Härter, Bettina and van Haaften-Visser, Désirée Y and van der Doef, Hubert P.J and van Hoesel, Marliek and Kansu, Aydan and van Vugt, Anke H.M and Thian, Marini and Kokke, Freddy T.M and Krolo, Ana and Başaran, Meryem Keçeli and Kaya, Neslihan Gurcan and Aksu, Aysel Ünlüsoy and Dalgıç, Buket and Ozcay, Figen and Baris, Zeren and Kain, Renate and Stigter, Edwin C.A and Lichtenbelt, Klaske D and Massink, Maarten P.G and Duran, Karen J and Verheij, Joke B.G.M and Lugtenberg, Dorien and Nikkels, Peter G.J and Brouwer, Henricus G.F and Verkade, Henkjan J and Scheenstra, René and Spee, Bart and Nieuwenhuis, Edward E.S and Coffer, Paul J and Janecke, Andreas R and van Haaften, Gijs and Houwen, Roderick H.J and Müller, Thomas and Middendorp, Sabine and Boztug, Kaan
Gastroenterology, ISSN 0016-5085, 07/2018, Volume 155, Issue 1, pp. 130 - 143.e15
Congenital diarrheal disorders are rare inherited intestinal disorders characterized by intractable, sometimes life-threatening, diarrhea and nutrient... 
PLE | 3-D Culture Model | CDD | Genomic | COA-DIACYLGLYCEROL ACYLTRANSFERASE-1 | HUMANS | FAMILY | COMBINED IMMUNODEFICIENCY | OBESITY RESISTANCE | MUTATION | DISEASE | DISORDER | PROTEIN-LOSING ENTEROPATHY | ABSORPTION | GASTROENTEROLOGY & HEPATOLOGY | CDD, congenital diarrheal disorder | BSA, bovine serum albumin | DG, diacylglycerol | GI, gastrointestinal | WT, wild-type | SSC, Side Scatter | cDNA, complementary DNA | hSI-EM, human small intestine expansion medium | PB, PiggyBac transposon | FFA, free fatty acid | OA, oleic acid | PBS, phosphate-buffered saline | TG, triacylglycerol | PLE, protein-losing enteropathy | DGAT1, diacylglycerol-acyltransferase 1 | sgRNA, single-guide RNA | B-LCL, B lymphoblastoid cell line
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text EVALUATION OF HUMAN LEUKOCYTE ANTIGEN CLASS I AND II ANTIGENS IN HELICOBACTER PYLORI-POSITIVE PEDIATRIC PATIENTS WITH ACTIVE GASTRITIS AND DUODENAL ULCER
by Gönen, Sevim and Sari, Sinan and Kandur, Yaşar and Dalgiç, Buket and Söylemezoğlu, Oğuz
Arquivos de gastroenterologia, ISSN 0004-2803, 12/2017, Volume 54, Issue 4, pp. 297 - 299
As being the first bacteria determined to be carcinogenic, Helicobacter pylori (H. pylori) is a pathogen localized in the stomach in more than half of the... 
Duodenal Ulcer - immunology | Humans | Histocompatibility Antigens Class I - immunology | Helicobacter Infections - complications | Male | Helicobacter Infections - immunology | Case-Control Studies | Histocompatibility Antigens Class II - immunology | Helicobacter pylori | Gastritis - immunology | Gastritis - microbiology | Female | Child | Index Medicus | Antígenos HLA | Úlcera duodenal | Gastrite | Criança
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text CD55 Deficiency, Early-Onset Protein-Losing Enteropathy, and Thrombosis
by Ozen, Ahmet and Comrie, William A and Ardy, Rico C and Domínguez Conde, Cecilia and Dalgic, Buket and Beser, Ömer F and Morawski, Aaron R and Karakoc-Aydiner, Elif and Tutar, Engin and Baris, Safa and Baris, Zeren and Ozcay, Figen and Serwas, Nina K and Zhang, Yu and Matthews, Helen F and Pittaluga, Stefania and Folio, Les R and Unlusoy Aksu, Aysel and McElwee, Joshua J and Krolo, Ana and Kiykim, Ayca and Gulsan, Meltem and Ogulur, Ismail and Snapper, Scott B and Houwen, Roderick H.J and Leavis, Helen L and Ertem, Deniz and Kain, Renate and Sari, Sinan and Erkan, Tülay and Su, Helen C and Boztug, Kaan and Lenardo, Michael J
The New England Journal of Medicine, ISSN 0028-4793, 07/2017, Volume 377, Issue 1, pp. 52 - 61
CD55 prevents convertase enzyme formation in the complement cascade, acting as a brake on complement activation. Inactivating mutations in CD55 result in... 
Protein-Losing Enteropathies | Complement Activation | Intestine, Small | T-Lymphocytes | Humans | Child, Preschool | Complement Inactivating Agents | Infant | Male | Immunoglobulin A | Thrombosis | Syndrome | Journal Article | Complement System Proteins | Homozygote | Pedigree | Statistics, Nonparametric | Female | Mutation | CD55 Antigens | Child | MEDICINE, GENERAL & INTERNAL | ACTIVATION | INFLAMMATORY-BOWEL-DISEASE | HEMOLYTIC-UREMIC SYNDROME | CELL RESPONSES | COMPLEMENT REGULATORY PROTEIN | INAB PHENOTYPE | DECAY-ACCELERATING FACTOR | PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA | MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS | T-CELLS | Intestine, Small - pathology | CD55 Antigens - genetics | Protein-Losing Enteropathies - genetics | Complement System Proteins - metabolism | CD55 Antigens - blood | Complement Activation - genetics | T-Lymphocytes - metabolism | Complement Inactivating Agents - pharmacology | Protein-Losing Enteropathies - complications | Immunoglobulin A - blood | Thrombosis - genetics | Complement Activation - drug effects | Proteins | Molecular targeted therapy | Gene mutations | Gastrointestinal diseases | Analysis | Homeostasis | Research | Blood clot | Gastrointestinal tract diseases | Complement component C5a | Lymphocytes T | Cell activation | Immunology | Pain | Intestine | Hepatology | Gastroenterology | Malabsorption | Thromboembolism | Digestive tract | Age | Edema | Medical research | Lymphatic system | Hypersensitivity | Diarrhea | Inflammation | Heredity | Protein deficiency | Patients | Hereditary diseases | Complement activation | Infectious diseases | Decay-accelerating factor
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Correction to: Molecular characterization of a human group C rotavirus detected first in Turkey
by Mitui, Marcelo Takahiro and Bozdayi, Gulendam and Dalgic, Buket and Bostanci, Ilknur and Nishizono, Akira and Ahmed, Kamruddin
Virus Genes, ISSN 0920-8569, 8/2018, Volume 54, Issue 4, pp. 621 - 621
This article was unintentionally published twice in this journal, by the same authors. Following should be considered the version of record and used for... 
Medical Microbiology | Biomedicine | Plant Sciences | Virology | Medical colleges | Viruses
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text Recurrent recessive mutation in deoxyguanosine kinase causes idiopathic noncirrhotic portal hypertension
by Vilarinho, Sílvia and Sari, Sinan and Yilmaz, Güldal and Stiegler, Amy L and Boggon, Titus J and Jain, Dhanpat and Akyol, Gulen and Dalgic, Buket and Günel, Murat and Lifton, Richard P
Hepatology, ISSN 0270-9139, 06/2016, Volume 63, Issue 6, pp. 1977 - 1986
Despite advances in the diagnosis and management of idiopathic noncirrhotic portal hypertension, its pathogenesis remains elusive. Insight may be gained from... 
MITOCHONDRIAL-DNA DEPLETION | LIVER-TRANSPLANTATION | DIDANOSINE | ANTIRETROVIRAL THERAPY | HEPATOPORTAL SCLEROSIS | GASTROENTEROLOGY & HEPATOLOGY | CHILDHOOD | ASSOCIATION | FAILURE | DEFICIENCY | FEATURES | Hypertension, Portal - genetics | Amino Acid Sequence | Humans | Child, Preschool | Molecular Sequence Data | Rats | Infant | Male | Phosphotransferases (Alcohol Group Acceptor) - genetics | Liver Failure - genetics | Genes, Recessive | Young Adult | Homozygote | Animals | Cattle | DNA Mutational Analysis | Pedigree | Adolescent | Dogs | Female | Child | Principal Component Analysis | Hypertension | Mutation | Hemorrhage | Liver | Rodents | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
10. Full Text Successful Treatment of Paecilomyces variotii Peritonitis in a Liver Transplant Patient
by Polat, Meltem and Kara, Soner Sertan and Tapısız, Anıl and Demirtaş, Zeliha and Sarı, Sinan and Kalkancı, Ayşe and Tezer, Hasan and Dalgıç, Buket
Mycopathologia, ISSN 0301-486X, 2015, Volume 179, Issue 3-4, pp. 317 - 320
Paecilomyces variotii has previously been reported as a causative pathogen for peritonitis in patients on continuous ambulatory peritoneal dialysis and shown... 
Liver transplant | Amphotericin B | Paecilomyces variotii peritonitis | Voriconazole | MYCOLOGY | Liver Transplantation - adverse effects | Humans | Mycoses - microbiology | Male | Paecilomyces - drug effects | Peritonitis - microbiology | Voriconazole - administration & dosage | Postoperative Complications - microbiology | Adolescent | Mycoses - drug therapy | Paecilomyces - isolation & purification | Peritonitis - drug therapy | Postoperative Complications - drug therapy | Paecilomyces - genetics | Antifungal Agents - administration & dosage | Infection | Care and treatment | Liver | Antiparasitic agents | Transplantation | Health aspects | Peritonitis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
11. Full Text High incidence of co-existing factors significantly modifying the phenotype in patients with Fabry disease
by Koca, Serhat and Tümer, Leyla and Okur, İlyas and Erten, Yasemin and Bakkaloğlu, Sevcan and Biberoğlu, Gürsel and Kasapkara, Çiğdem and Küçükçongar, Aynur and Dalgıç, Buket and Oktar, Suna Özhan and Öner, Yusuf and Atalay, Tuba and Cemri, Mustafa and Çiftçi, Bahattin and Topçu, Burcu and Hasanoğlu, Alev and Ezgü, Fatih
Gene, ISSN 0378-1119, 03/2019, Volume 687, pp. 280 - 288
Fabry disease results from deficiency of the lysosomal enzyme alpha-galactosidase A. The families of 11 index cases were screened by enzyme and molecular... 
Fabry disease | X-inactivation | Phenotype modifiers | Family screening | DIAGNOSIS | HOMOCYSTEINE | INVOLVEMENT | GALACTOSIDASE-A GENE | PREVALENCE | NATURAL-HISTORY | IMPACT | GENETICS & HEREDITY | MUTATIONS | ALPHA-GALACTOSIDASE | MANIFESTATIONS | Biomarkers - metabolism | alpha-Galactosidase - genetics | Prognosis | Fabry Disease - epidemiology | Follow-Up Studies | Humans | Middle Aged | Risk Factors | Child, Preschool | Male | alpha-Galactosidase - metabolism | Case-Control Studies | Genetic Variation | Young Adult | Phenotype | Turkey - epidemiology | Pedigree | Fabry Disease - metabolism | Adolescent | Adult | Female | Heterozygote | Child | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
12. Full Text A Successful HSCT in a Girl with Novel LRBA Mutation with Refractory Celiac Disease
by Sari, Sinan and Sari, Sinan and Dogu, Figen and Dogu, Figen and Hwa, Vivian and Hwa, Vivian and Haskologlu, Sule and Haskologlu, Sule and Dauber, Andrew and Dauber, Andrew and Rosenfeld, Ron and Rosenfeld, Ron and Polat, Meltem and Polat, Meltem and Kuloglu, Zarife and Kuloglu, Zarife and Kansu, Aydan and Kansu, Aydan and Dalgic, Buket and Dalgic, Buket and Ikinciogullari, Aydan and Ikinciogullari, Aydan
Journal of Clinical Immunology, ISSN 0271-9142, 1/2016, Volume 36, Issue 1, pp. 8 - 11
Medical Microbiology | Infectious Diseases | Internal Medicine | Biomedicine | Immunology | IMMUNE DYSREGULATION | IMMUNOLOGY | AUTOIMMUNITY | DEFICIENCY | Recurrence | Humans | Hematopoietic Stem Cell Transplantation | Celiac Disease - diagnosis | Homozygote | DNA Mutational Analysis | Pedigree | Adaptor Proteins, Signal Transducing - genetics | Female | Consanguinity | Chimerism | Celiac Disease - therapy | Child | Drug Resistance | Frameshift Mutation - genetics | Prednisone - therapeutic use | College teachers
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
13. Full Text Multiple Presentations of LRBA Deficiency: a Single-Center Experience
by Kostel Bal, Sevgi and Haskologlu, Sule and Serwas, Nina K and Islamoglu, Candan and Aytekin, Caner and Kendirli, Tanil and Kuloglu, Zarife and Yavuz, Gulsan and Dalgic, Buket and Siklar, Zeynep and Kansu, Aydan and Ensari, Arzu and Boztug, Kaan and Dogu, Figen and Ikinciogullari, Aydan
Journal of Clinical Immunology, ISSN 0271-9142, 11/2017, Volume 37, Issue 8, pp. 790 - 800
LPS-responsive beige-like anchor protein (LRBA) deficiency is a primary immunodeficiency categorized as common variable immunodeficiency associated with... 
LRBA deficiency | ALPS | Medical Microbiology | Biomedicine | Immunology | autoimmunity | Infectious Diseases | Internal Medicine | HSCT | MUTATION | DISEASE | PATIENT | IMMUNOLOGY | STEM-CELL TRANSPLANTATION | Inflammatory Bowel Diseases - drug therapy | Common Variable Immunodeficiency - drug therapy | Humans | Immunosuppressive Agents - therapeutic use | Inflammatory Bowel Diseases - diagnosis | Common Variable Immunodeficiency - genetics | Infant | Male | Autoimmune Diseases - diagnosis | Mutation - genetics | Autoimmune Diseases - genetics | Common Variable Immunodeficiency - diagnosis | Disease-Free Survival | Homozygote | Turkey | Abatacept - therapeutic use | Adaptor Proteins, Signal Transducing - genetics | Adolescent | Fatal Outcome | Inflammatory Bowel Diseases - genetics | Female | Sepsis | Child | Autoimmune Diseases - drug therapy | Autoimmunity | Medical research | Gastrointestinal diseases | Analysis | Medicine, Experimental | Transplantation | Hematopoietic stem cells | Inflammatory bowel diseases | Immunological memory | Common variable immunodeficiency | Stem cell transplantation | Diarrhea | Hypogammaglobulinemia | Protein deficiency | Hemopoiesis | Lipopolysaccharides | Lymphocytes B | Intestine | Early experience | Differential diagnosis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
14. Tacrolimus-Induced Autoimmune Hemolytic Anemia in a Previously Reported Child With History of Thrombocytopenia Following Liver Transplant
by Kaya, Zühre and Egritas, Odul and Dalgic, Buket
Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, 06/2018, Volume 16, Issue 3, p. 355
Glucocorticoids - administration & dosage | Prednisone - administration & dosage | Liver Transplantation - adverse effects | Calcineurin Inhibitors - administration & dosage | Humans | Anemia, Hemolytic, Autoimmune - drug therapy | Child, Preschool | Anemia, Hemolytic, Autoimmune - chemically induced | Male | Treatment Outcome | Thrombocytopenia - chemically induced | Biomarkers - blood | Anemia, Hemolytic, Autoimmune - blood | Tacrolimus - adverse effects | Thrombocytopenia - blood | Calcineurin Inhibitors - adverse effects | Thrombocytopenia - drug therapy | Anemia, Hemolytic, Autoimmune - diagnosis | Immunosuppressive Agents - adverse effects | Thrombocytopenia - diagnosis | Immunosuppressive Agents - administration & dosage | Tacrolimus - administration & dosage
Journal Article
Details down arrow
15. Full Text Eponym
: Papillon–Lefevre syndrome
by Dalgıc, Buket and Dalgıc, Buket and Bukulmez, Aysegul and Bukulmez, Aysegul and Sarı, Sinan and Sarı, Sinan
European Journal of Pediatrics, ISSN 0340-6199, 6/2011, Volume 170, Issue 6, pp. 689 - 691
Papillon–Lefevre Syndrome (PLS) is a very rare autosomal recessive disorder characterized by palmoplantar hyperkeratosis and severe early onset periodontitis,... 
Pediatrics | Cathepsin C gene | Papillon–Lefevre syndrome | Medicine & Public Health | Periodontitis | Palmoplantar keratosis | Papillon-Lefevre syndrome | LOCALIZATION | CATHEPSIN-C GENE | PEDIATRICS | MUTATIONS | ETRETINATE TREATMENT | Point Mutation | Papillon-Lefevre Disease - diagnosis | Prognosis | Humans | Cathepsin C - genetics | Papillon-Lefevre Disease - genetics | Eponyms | Papillon-Lefevre Disease - therapy | Child | Early Diagnosis | Cathepsins | Home care | Universities and colleges | Gene mutations
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
16. Tacrolimus-induced autoimmune hemolytic anemia in a previously reported child with history of thrombocytopenia following liver transplant
by Kaya, Zühre and Egritas, Odul and Dalgic, Buket
Experimental and Clinical Transplantation, ISSN 1304-0855, 06/2018, Volume 16, Issue 3, pp. 355 - 356
SOLID-ORGAN TRANSPLANT | TRANSPLANTATION
Journal Article
Details down arrow