Zobrazeno 1 - 10
of 10
pro vyhledávání: '"M A, Yeşilipek"'
Autor:
Vural Kesik, Erman Ataş, Musa Karakükcü, Serap Aksoylar, Fatih Erbey, Nurdan Taçyıldız, Alphan Küpesiz, Haldun Öniz, Ekrem Ünal, Savaş Kansoy, Gülyüz Öztürk, Murat Elli, Zühre Kaya, Emel Ünal, Volkan Hazar, Şebnem Yılmaz Bengoa, Gülsün Karasu, Didem Atay, Ayhan Dağdemir, Hale Ören, Ülker Koçak, M. Akif Yeşilipek
Publikováno v:
Turkish Journal of Hematology, Vol 33, Iss 4, Pp 265-272 (2016)
Objective: The prognostic factors and a new childhood prognostic index after autologous hematopoietic stem cell transplantation (AHSCT) in patients with relapsed/refractory Hodgkin's lymphoma (HL) were evaluated. Materials and Methods: The prognostic
Externí odkaz:
https://doaj.org/article/11710a1ff4ac45be8d3597fa515fe8ab
Publikováno v:
Turkish Journal of Hematology, Vol 33, Iss 2, Pp 107-111 (2016)
INTRODUCTION: Although the calculated carrier frequency for point mutations of the β-globin gene is around 10% for Antalya Province, nothing is known about the profile of large deletional mutations involving the β-globin gene. In this study, we aim
Externí odkaz:
https://doaj.org/article/8b4aa288826c4489ab0cc4efc4a2b02c
Autor:
M. Akif Yeşilipek
Publikováno v:
Volume: 23, Issue: 1 49-59
Arşiv Kaynak Tarama Dergisi
Arşiv Kaynak Tarama Dergisi
Hemoglobinopathies include an enormous patient population in south part of Turkey. Allogeneic hematopoietic stem cell transplantation is only curative treatment in thalassemia. Optimal medical therapy is very important in the years before transplant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e1a33eac5f2cd1adf8d799db32ceb7d
https://doi.org/10.17827/aktd.22596
https://doi.org/10.17827/aktd.22596
Publikováno v:
The Turkish journal of pediatrics. 41(1)
We present a seven-month-old boy referred to our hospital with a history of recurrent suppurative infections starting in his neonatal period. Anemia, absolute neutropenia absolute neutrophil count (ANC: 500 cells/microl), pneumonia, purulent otitis m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ae735f3d779901909c51ad2254efa85b
https://pubmed.ncbi.nlm.nih.gov/10770686
https://pubmed.ncbi.nlm.nih.gov/10770686
Publikováno v:
Acta haematologica. 100(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::603839ce345643050e44afa0cf6c8922
https://pubmed.ncbi.nlm.nih.gov/9858797
https://pubmed.ncbi.nlm.nih.gov/9858797
Publikováno v:
The Turkish journal of pediatrics. 38(3)
A case of Bernard-Soulier syndrome in a five-year-old female is presented. The diagnosis was confirmed by flow cytometric analysis of glycoprotein Ib (CD 42b) in addition to the patient's classic laboratory findings such as prolonged bleeding time, m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2a3bf432163b6bd8395abd56ea811214
https://pubmed.ncbi.nlm.nih.gov/8827910
https://pubmed.ncbi.nlm.nih.gov/8827910
Publikováno v:
Acta haematologica. 92(1)
Monosomy 7 myelodysplasia is a rare hematological entity and is associated with morphological abnormalities in bone marrow and peripheral smear, and poor prognosis in children. We describe 2 children with infantile monosomy 7 myelodysplasia which evo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::505d9a16bbf2090b7094c2041c1e1a01
https://pubmed.ncbi.nlm.nih.gov/7985480
https://pubmed.ncbi.nlm.nih.gov/7985480
Publikováno v:
The Turkish journal of pediatrics. 34(4)
Cytogenetic abnormalities are rarely found in patients with juvenile chronic myelogenous leukemia (JCML). In patients with chromosomal abnormalities, chromosomes 7 and 8 are usually involved. A case of JCML with 47 XXX and a 46 XX karyotype is descri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::271ad933a47e3be3afa0a0738e459937
https://pubmed.ncbi.nlm.nih.gov/1306346
https://pubmed.ncbi.nlm.nih.gov/1306346
Autor:
M A, Yeşilipek
Publikováno v:
The Turkish journal of pediatrics. 34(1)
The study population consisted of 22 infants hospitalized for low birth weight or prematurity at the Maternity and Children's Hospital in Samsun. Eleven infants were fed the low birth weight formula and the rest were fed the standard formula. Weight
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d78663a428252abe425e5803fb2628e0
https://pubmed.ncbi.nlm.nih.gov/1509527
https://pubmed.ncbi.nlm.nih.gov/1509527
Autor:
Öztürk, Zeynep
YEN DOĞANLARDA ORAK HÜCRE ANEM S N NTARANMASIZEYNEP ÖZTÜRKDünyada yaygın olarak görülen hemoglobinopatiler hemoglobinmolekülünün genetik bozukluklarıdır. Hb S en yaygın hemoglobin varyantıdırve β-globin zincirinin altıncı pozisyo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c2ec27bb35614f291861c8a9099e950e
https://acikbilim.yok.gov.tr/handle/20.500.12812/31384
https://acikbilim.yok.gov.tr/handle/20.500.12812/31384
