Found: 55
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Serum transferrin receptor in children and adolescents with inflammatory bowel disease.
- Published in:
- 2000
- By:
- Publication type:
- journal article
Cdan1 Is Essential for Primitive Erythropoiesis.
- Published in:
- Frontiers in Physiology, 2021, v. 12, p. 1, doi. 10.3389/fphys.2021.685242
- By:
- Publication type:
- Article
Symptomatic corpus luteum hemorrhage in adolescent females with ITP.
- Published in:
- European Journal of Pediatrics, 2024, v. 183, n. 7, p. 2893, doi. 10.1007/s00431-024-05560-0
- By:
- Publication type:
- Article
Emergency or urgent splenectomy in children for non-traumatic reasons.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Distal limb anomalies in patients with congenital dyserythropoietic anemia.
- Published in:
- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 2, p. 487, doi. 10.1002/ajmg.a.38012
- By:
- Publication type:
- Article
Biallelic hypomorphic variants in CAD cause uridine‐responsive macrocytic anaemia with elevated haemoglobin‐A2.
- Published in:
- British Journal of Haematology, 2024, v. 204, n. 3, p. 1067, doi. 10.1111/bjh.19215
- By:
- Publication type:
- Article
Incorporation of somatic panels for the detection of haematopoietic transformation in children and young adults with leukaemia predisposition syndromes and with acquired cytopenias.
- Published in:
- British Journal of Haematology, 2021, v. 193, n. 3, p. 570, doi. 10.1111/bjh.17285
- By:
- Publication type:
- Article
Splenectomy in childhood for non‐malignant haematologic disorders – long‐term follow‐up shows minimal adverse effects.
- Published in:
- British Journal of Haematology, 2020, v. 190, n. 6, p. 909, doi. 10.1111/bjh.16657
- By:
- Publication type:
- Article
Prothrombotic Factors in Children with Otitis Media and Sinus Thrombosis.
- Published in:
- Laryngoscope, 2004, v. 114, n. 1, p. 90
- By:
- Publication type:
- Article
A Need for a Novel Survival Risk Scoring System for Intensive Care Admissions Due to Sepsis in Pediatric Hematology/Oncology Patients.
- Published in:
- Journal of Intensive Care Medicine, 2024, v. 39, n. 5, p. 484, doi. 10.1177/08850666231216362
- By:
- Publication type:
- Article
Anemia and markers of erythropoiesis in pediatric kidney transplant recipients compared to children with chronic renal failure.
- Published in:
- Pediatric Transplantation, 2016, v. 20, n. 7, p. 958, doi. 10.1111/petr.12792
- By:
- Publication type:
- Article
CATSPER2, a human autosomal nonsyndromic male infertility gene.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 7, p. 497, doi. 10.1038/sj.ejhg.5200991
- By:
- Publication type:
- Article
Characterization of the interactions between Codanin-1 and C15Orf41, two proteins implicated in congenital dyserythropoietic anemia type I disease.
- Published in:
- BMC Molecular & Cell Biology, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12860-020-00258-1
- By:
- Publication type:
- Article
Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias.
- Published in:
- European Journal of Haematology, 2018, v. 101, n. 3, p. 297, doi. 10.1111/ejh.13097
- By:
- Publication type:
- Article
Morphological features of congenital dyserythropoietic anemia type I: The role of electron microscopy in diagnosis.
- Published in:
- European Journal of Haematology, 2017, v. 99, n. 4, p. 366, doi. 10.1111/ejh.12931
- By:
- Publication type:
- Article
Molecular diagnosis of α-thalassemia in a multiethnic population.
- Published in:
- European Journal of Haematology, 2017, v. 98, n. 6, p. 553, doi. 10.1111/ejh.12866
- By:
- Publication type:
- Article
Morbidity and mortality of adult patients with congenital dyserythropoietic anemia type I.
- Published in:
- European Journal of Haematology, 2017, v. 98, n. 1, p. 13, doi. 10.1111/ejh.12778
- By:
- Publication type:
- Article
A novel epsilon gamma delta beta thalassemia presenting with pregnancy complications and severe neonatal anemia.
- Published in:
- European Journal of Haematology, 2013, v. 90, n. 2, p. 127, doi. 10.1111/ejh.12047
- By:
- Publication type:
- Article
High levels of soluble serum hemojuvelin in patients with congenital dyserythropoietic anemia type I.
- Published in:
- European Journal of Haematology, 2013, v. 90, n. 1, p. 31, doi. 10.1111/ejh.12027
- By:
- Publication type:
- Article
Pregnancy outcome in congenital dyserythropoietic anemia type I.
- Published in:
- European Journal of Haematology, 2008, v. 81, n. 4, p. 317, doi. 10.1111/j.1600-0609.2008.01109.x
- By:
- Publication type:
- Article
Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients.
- Published in:
- European Journal of Haematology, 2005, v. 74, n. 2, p. 93, doi. 10.1111/j.1600-0609.2004.00371.x
- By:
- Publication type:
- Article
Molecular characterization of three novel Fanconi anemia mutations in Israeli Arabs.
- Published in:
- European Journal of Haematology, 2004, v. 72, n. 5, p. 330, doi. 10.1111/j.1600-0609.2004.00240.x
- By:
- Publication type:
- Article
International Forum.
- Published in:
- Vox Sanguinis, 2001, v. 80, n. 2, p. 132, doi. 10.1046/j.1423-0410.2001.00022-9.x
- By:
- Publication type:
- Article
Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Congenital Anemias.
- Published in:
- Molecular Diagnosis & Therapy, 2020, v. 24, n. 4, p. 397, doi. 10.1007/s40291-020-00478-3
- By:
- Publication type:
- Article
Consensus Paper-ICIS Expert Meeting Basel 2009 treatment milestones in immune thrombocytopenia.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Association between childhood nephrotic syndrome and hemophagocytic lymphohistiocytosis.
- Published in:
- 2013
- By:
- Publication type:
- Report
Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE).
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 1, p. 133, doi. 10.1093/hmg/ddy334
- By:
- Publication type:
- Article
Pediatric myelodysplastic syndrome with inflammatory manifestations: Diagnosis, genetics, treatment, and outcome.
- Published in:
- Pediatric Blood & Cancer, 2021, v. 68, n. 10, p. 1, doi. 10.1002/pbc.29138
- By:
- Publication type:
- Article
Congenital neutropenia with variable clinical presentation in novel mutation of the SRP54 gene.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Essential thrombocythemia A retrospective case series.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Patient and central venous catheter related risk factors for blood stream infections in children receiving chemotherapy.
- Published in:
- Pediatric Blood & Cancer, 2015, v. 62, n. 3, p. 471, doi. 10.1002/pbc.25281
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- Publication type:
- Article
Genetic analysis and clinical picture of severe congenital neutropenia in Israel.
- Published in:
- Pediatric Blood & Cancer, 2015, v. 62, n. 1, p. 103, doi. 10.1002/pbc.25251
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- Publication type:
- Article
A comparative prospective observational study of children and adults with immune thrombocytopenia: 2‐year follow‐up.
- Published in:
- American Journal of Hematology, 2018, v. 93, n. 6, p. 751, doi. 10.1002/ajh.25086
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- Publication type:
- Article
Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian population.
- Published in:
- American Journal of Hematology, 2011, v. 86, n. 9, p. 727, doi. 10.1002/ajh.22096
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- Publication type:
- Article
Genetic variants in the noncoding region of RPS19 gene in Diamond-Blackfan anemia: Potential implications for phenotypic heterogeneity.
- Published in:
- American Journal of Hematology, 2010, v. 85, n. 2, p. 111, doi. 10.1002/ajh.21601
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- Publication type:
- Article
IGF-I treatment of patients with Laron syndrome suppresses serum thrombopoietin levels but does not affect serum erythropoietin.
- Published in:
- American Journal of Hematology, 2009, v. 84, n. 1, p. 64, doi. 10.1002/ajh.21318
- By:
- Publication type:
- Article
Response to hydroxyurea therapy in β-thalassemia.
- Published in:
- American Journal of Hematology, 2008, v. 83, n. 5, p. 366, doi. 10.1002/ajh.21120
- By:
- Publication type:
- Article
Hypocholesterolemia in chronic anemias with increased erythropoietic activity.
- Published in:
- American Journal of Hematology, 2007, v. 82, n. 3, p. 199, doi. 10.1002/ajh.20804
- By:
- Publication type:
- Article
Hydrops fetalis associated with homozygosity for hemoglobin Taybe (α 38/39 THR deletion) in newborn triplets.
- Published in:
- American Journal of Hematology, 2004, v. 76, n. 3, p. 263, doi. 10.1002/ajh.20094
- By:
- Publication type:
- Article
How high are carrier frequencies of rare recessive syndromes? Contemporary estimates for Fanconi Anemia in the United States and Israel.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 8, p. 1877, doi. 10.1002/ajmg.a.34087
- By:
- Publication type:
- Article
A randomized phase II trial of Arginine Butyrate with standard local therapy in refractory sickle cell leg ulcers.
- Published in:
- British Journal of Haematology, 2010, v. 151, n. 5, p. 516, doi. 10.1111/j.1365-2141.2010.08395.x
- By:
- Publication type:
- Article
Clinical and molecular variability in congenital dyserythropoietic anaemia type I.
- Published in:
- British Journal of Haematology, 2005, v. 130, n. 4, p. 628, doi. 10.1111/j.1365-2141.2005.05642.x
- By:
- Publication type:
- Article
Glycoconjugate abnormalities in patients with congenital dyserythropoietic anaemia type I, II and III.
- Published in:
- British Journal of Haematology, 2001, v. 114, n. 4, p. 907, doi. 10.1046/j.1365-2141.2001.03046.x
- By:
- Publication type:
- Article
Small-platelet thrombocytopenia in a family with autosomal recessive inheritance pattern.
- Published in:
- Pediatric Blood & Cancer, 2013, v. 60, n. 10, p. E128, doi. 10.1002/pbc.24581
- By:
- Publication type:
- Article
Steroid therapy may be effective in augmenting hemoglobin levels during hemolytic crises in children with hereditary spherocytosis.
- Published in:
- Pediatric Blood & Cancer, 2011, v. 57, n. 2, p. 303, doi. 10.1002/pbc.22844
- By:
- Publication type:
- Article
Remission from transfusion-dependence in a patient with congenital dyserythropoietic anemia (CDA) and increased intensity of iron chelation.
- Published in:
- Pediatric Blood & Cancer, 2009, v. 53, n. 6, p. 1167, doi. 10.1002/pbc.22204
- By:
- Publication type:
- Article
Risk factors for future development of systemic lupus erythematosus in children with idiopathic thrombocytopenic purpura.
- Published in:
- Pediatric Blood & Cancer, 2006, v. 47, n. S5, p. 657, doi. 10.1002/pbc.20970
- By:
- Publication type:
- Article
Characterization of Fanconi Anemia Patients with Head and Neck Squamous Cell Carcinoma: Israel Fanconi Registry.
- Published in:
- Israel Medical Association Journal, 2022, v. 24, n. 8, p. 491
- By:
- Publication type:
- Article
Resolving a genetic paradox throughout preimplantation genetic diagnosis for autosomal dominant severe congenital neutropenia.
- Published in:
- Prenatal Diagnosis, 2010, v. 30, n. 3, p. 207, doi. 10.1002/pd.2437
- By:
- Publication type:
- Article
Alpha-Thalassemia Carrier due to –α<sup>3.7</sup> Deletion: Not So Silent.
- Published in:
- Acta Haematologica, 2020, v. 143, n. 5, p. 432, doi. 10.1159/000503023
- By:
- Publication type:
- Article