Zobrazeno 1 - 10
of 255
pro vyhledávání: '"Kostmann syndrome"'
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Background: Severe congenital neutropenia (SCN), also known as Kostmann syndrome, is a rare heterogeneous group of diseases characterized by arrested neutrophil maturation in the bone marrow.Case Presentation: We report a case of Kostmann syndrome an
Externí odkaz:
https://doaj.org/article/1e357815ef4d46069d302c4db867c08e
Publikováno v:
Volume: 16, Issue: 2 160-164
Türkiye Çocuk Hastalıkları Dergisi
Türkiye Çocuk Hastalıkları Dergisi
Ağır konjenital nötropeniler (AKN), nadir görülen olgun nötrofillerin eksikliği ile karakterize primer bir immün yetersizlik hastalığıdır. Klinik özellikler arasında doğumdan itibaren azalmış mutlak nötrofil sayısı, tekrarlayan ve
Autor:
Seçil Çalişkan, Canan Özdemir
Publikováno v:
OSMANGAZİ JOURNAL OF MEDICINE. 42:260-264
Publikováno v:
Sohag Medical Journal. 24:1-10
Kostmann syndrome is a rare congenital disorder characterized by severe neutropenia due to impairment of myeloid differentiation in the bone marrow, with the neutrophil count being characteristically less than 500_103 cells/lMale child 4.5-year old c
Publikováno v:
The American Journal of Case Reports
Patient: Female, 32 Final Diagnosis: Papillary thyroid carcinoma Symptoms: Cervical node metastasis Medication: — Clinical Procedure: Radioactive iodine treatment Specialty: Oncology Objective: Rare co-existance of disease or pathology Background:
Autor:
Ebru Canda, Hüseyin Onay, Sema Kalkan Uçar, Eser Yıldırım Sözmen, Ferda Ozkinay, Mehtap Kagnici, Melis Köse, Deniz Yilmaz Karapinar, Mahmut Çoker
Publikováno v:
Blood Cells, Molecules, and Diseases. 76:1-6
WOS: 000461043500001
PubMed ID: 30473482
Gaucher Disease (GD) is the most common lysosomal storage disorder has traditionally been classified into three clinical phenotypes. Type 3 GD is characterized by neurological involvement but neurolo
PubMed ID: 30473482
Gaucher Disease (GD) is the most common lysosomal storage disorder has traditionally been classified into three clinical phenotypes. Type 3 GD is characterized by neurological involvement but neurolo
Publikováno v:
Journal of Medical Microbiology. 68:609-615
Purpose. The oral microbiome is maintained by host- and microbe-derived factors. A shift in microbial composition, as a result of diseases related to the immune system, is the most important step in the development of oral and dental diseases. The ai
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Autor:
Christoph Klein
Publikováno v:
Stiehm's Immune Deficiencies ISBN: 9780128167687
Congenital neutropenia (CN) comprises a heterogeneous group of genetically determined disorders characterized by a decrease of neutrophil granulocytes in the peripheral blood. Low numbers of neutrophil granulocytes predispose to severe and recurrent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28d4b0fc1f0dac9fbc76f723b1eeeb95
https://doi.org/10.1016/b978-0-12-816768-7.00035-1
https://doi.org/10.1016/b978-0-12-816768-7.00035-1
Autor:
Nima Rezaei
Publikováno v:
Pediatric Immunology ISBN: 9783030212612
A hypocellular bone marrow with isolated decrease in myeloid precursors, and early onset low neutrophil count below 500/μL, are suggestive of congenital neutropenia Congenital neutropenia often refers to severe congenital neutropenia (SCN), subsumin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6cf43f32136039c781ddd5ef3fc4fdb
https://doi.org/10.1007/978-3-030-21262-9_51
https://doi.org/10.1007/978-3-030-21262-9_51