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Seminars in Hematology, ISSN 0037-1963, 01/2013, Volume 50, Issue 1, pp. S71 - S74
Although the majority of children with immune thrombocytopenia (ITP) have a short duration of the disease, the very rare but significant complications of the... 
Prognosis | Prospective Studies | Humans | Thrombocytopenia - immunology | Biomarkers - analysis | Child, Preschool | Quality of Life | Child
Journal Article
Blood, ISSN 0006-4971, 11/2018, Volume 132, Issue Supplement 1, pp. 4940 - 4940
Abstract Background: Autoimmune neutropenia of infancy (AIN), the most frequent type of severe neutropenia in young children, occurs due to recognition of... 
Journal Article
Blood, ISSN 0006-4971, 12/2014, Volume 124, Issue 21, pp. 4895 - 4895
Abstract Background: The prolonged survival in patients with beta thalassemia major and other transfusion dependent disorders has exposed the multi-organ... 
Journal Article
Journal of Child Neurology, ISSN 0883-0738, 3/2019, Volume 34, Issue 3, pp. 121 - 127
This study sought to investigate the need for thrombophilia screening in pediatric migraineurs. The cohort included 45/824 children (5.5%) aged 3-18 years with... 
migraine with aura | adolescents | lipoprotein(a) | thrombophilia testing | migraine without aura | pediatric | POLYMORPHISM | MTHFR GENE | CLINICAL NEUROLOGY | LIPOPROTEIN | WOMEN | PEDIATRICS | ISCHEMIC-STROKE | ASSOCIATION
Journal Article
Blood, ISSN 0006-4971, 12/2016, Volume 128, Issue 22, pp. 3585 - 3585
Abstract Elective splenectomy in childhood can ameliorate the clinical manifestations of non-malignant hematological diseases such as beta-thalassemia,... 
Journal Article
European Journal of Haematology, ISSN 0902-4441, 09/2018, Volume 101, Issue 3, pp. 297 - 304
Background Most patients with anemia are diagnosed through clinical phenotype and basic laboratory testing. Nonetheless, in cases of rare congenital anemias,... 
red cell disorders | DYSERYTHROPOIETIC ANEMIA | HEREDITARY STOMATOCYTOSIS | GENE | RECOMMENDATIONS | PIEZO1 | PYRUVATE-KINASE DEFICIENCY | SPLENECTOMY | MUTATIONS | HEMATOLOGY | BONE-MARROW FAILURE | NONSPHEROCYTIC HEMOLYTIC-ANEMIA | Genetic Testing | Anemia - blood | Anemia, Hemolytic, Congenital Nonspherocytic - diagnosis | Humans | Anemia, Dyserythropoietic, Congenital - diagnosis | Child, Preschool | Pyruvate Metabolism, Inborn Errors - genetics | Erythrocyte Indices | Male | Young Adult | Hydrops Fetalis - genetics | Anemia, Sideroblastic - diagnosis | Pyruvate Metabolism, Inborn Errors - diagnosis | Adult | Female | Child | Genetic Predisposition to Disease | Anemia, Dyserythropoietic, Congenital - therapy | Genetic Association Studies | Hydrops Fetalis - diagnosis | Anemia - diagnosis | Anemia, Dyserythropoietic, Congenital - genetics | Computational Biology | Anemia - therapy | Rare Diseases | Anemia, Hemolytic, Congenital - genetics | Pyruvate Kinase - deficiency | Anemia - congenital | Anemia, Sideroblastic - genetics | Anemia, Hemolytic, Congenital - diagnosis | Bone Marrow - pathology | Adolescent | High-Throughput Nucleotide Sequencing | Mutation | Pyruvate Kinase - genetics | Anemia, Hemolytic, Congenital Nonspherocytic - genetics | Anemia | Genetic disorders | Medical genetics | Phenotypes | Genetic counseling | Pyruvate kinase | Pyruvic acid | Sideroblastic anemia | Diagnosis | Kinases | Genetic screening
Journal Article
Seminars in Hematology, ISSN 0037-1963, 04/2016, Volume 53, Issue 2, pp. S35 - S38
Journal Article
European Journal of Haematology, ISSN 0902-4441, 06/2017, Volume 98, Issue 6, p. 553
[alpha]-Thalassemia, one of the most common genetic diseases, is caused by deletions or point mutations affecting one to four [alpha]-globin genes. Molecular... 
Hemoglobin | Thalassemia | Algorithms | Diagnosis | Gene mutations | Analysis | Polymerase chain reaction | Laboratories | Anemia | Mutation
Journal Article
The Pediatric Infectious Disease Journal, ISSN 0891-3668, 02/2019, Volume 38, Issue 2, pp. 127 - 130
BACKGROUND:Valganciclovir (2/d) therapy for 6 months in neonates with symptomatic congenital cytomegalovirus (cCMV) infection improves hearing and... 
HEARING-LOSS | INFECTIOUS DISEASES | cytomegalovirus | congenital cytomegalovirus | LENTICULOSTRIATED VASCULOPATHY | INFANTS | valganciclovir | PEDIATRICS | IMMUNOLOGY | ORAL VALGANCICLOVIR | Hematologic agents | Cytomegalovirus infections | Health aspects
Journal Article
Journal of child neurology, 11/2018, p. 883073818811545
This study sought to investigate the need for thrombophilia screening in pediatric migraineurs. The cohort included 45/824 children (5.5%) aged 3-18 years with... 
Journal Article
Blood Cells, Molecules and Diseases, ISSN 1079-9796, 07/2018, Volume 71, pp. 1 - 4
Poor adherence of transfusion-dependent patients to chelation treatment is often the cause of persistent iron overload and ensuing morbidity. However, a tool... 
Iron overload | Chelation | Thalassemia | Labile plasma iron | Compliance | SERUM FERRITIN | OVERLOAD | DEFERASIROX | ANEMIAS | HEMATOLOGY
Journal Article
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 01/2015, Volume 62, Issue 1, pp. 103 - 108
Journal Article