Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Sakir, Altunbaşak"'
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 9, Iss 3, Pp 229-234 (2019)
INTRODUCTION: In this study, it was aimed to identify the clinical findings, treatment modalities and factors affecting the prognosis of patients who were followed up and treated with acute transverse myelitis. METHODS: A total of 17 patients diagnos
Externí odkaz:
https://doaj.org/article/108eded127354427bff5ebd315077d80
Publikováno v:
The Turkish journal of pediatrics. 55(5)
Ring chromosome 14 syndrome is a rare genetic disorder. Typically, children with this syndrome have distinct facial features, development delay, microcephaly, seizures, ocular abnormalities, and recurrent respiratory infections. Epilepsy associated w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e83afafed2bcde8e11dca9aa5752a2c7
https://pubmed.ncbi.nlm.nih.gov/24382541
https://pubmed.ncbi.nlm.nih.gov/24382541
Publikováno v:
The Turkish journal of pediatrics. 54(5)
Topiramate is one of the newer generation antiepileptic drugs with a beneficial clinical effect on various seizure types. In this study, we present the clinical findings of hypohidrosis and hyperthermia with topiramate in pediatric patients. The data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e02e3b4f5644f8b00487843964e70872
https://pubmed.ncbi.nlm.nih.gov/23427516
https://pubmed.ncbi.nlm.nih.gov/23427516
Publikováno v:
The Turkish journal of pediatrics. 53(1)
Pseudotumor cerebri (PTC) is a clinical condition characterized by signs and symptoms of increased intracranial pressure, such as headache and papilledema. A total of 16 patients diagnosed with PTC [12 (75%) female; 4 (25%) male] were included in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::87c16cdb1239fa7ea871bac1226c1dfa
https://pubmed.ncbi.nlm.nih.gov/21534340
https://pubmed.ncbi.nlm.nih.gov/21534340
Publikováno v:
The Turkish journal of pediatrics. 52(5)
Hyperimmunoglobulin E syndrome (HIES) is recognized as a multisystem disorder with various connective tissue, skeletal and immunologic abnormalities. Central nervous system abnormalities have been considered a feature of HIES. Pseudotumor cerebri (PT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::352da05a667231e0b220ba0461c73f96
https://pubmed.ncbi.nlm.nih.gov/21434544
https://pubmed.ncbi.nlm.nih.gov/21434544
Publikováno v:
The Turkish journal of pediatrics. 52(1)
We report herein our interesting case series of 15 infants admitting with neurological symptoms who were found to have vitamin B12 deficiency. Infants who were admitted to our hospital between 2004 and 2007 with neurological symptoms and were found t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::920d3983037d7f47cce9cdddfa162bcb
https://pubmed.ncbi.nlm.nih.gov/20402062
https://pubmed.ncbi.nlm.nih.gov/20402062
Autor:
Emel, Erdoğan-Bakar, Mine, Cinbiş, Hamit, Ozyürek, Nurcihan, Kiriş, Sakir, Altunbaşak, Banu, Anlar
Publikováno v:
The Turkish journal of pediatrics. 51(6)
Attention, learning, and perceptual problems have been reported at various degrees and rates in neurofibromatosis type 1 (NF1). We aimed to define the cognitive profiles frequently associated with NF1. Children and adolescents with NF1 (n=58) were te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::30f53a008aa8ecf956e0962b9b1743c0
https://pubmed.ncbi.nlm.nih.gov/20196390
https://pubmed.ncbi.nlm.nih.gov/20196390
Publikováno v:
The Turkish journal of pediatrics. 50(1)
Guillain-Barré syndrome is clinically characterized by acute onset of generalized, symmetrical, and ascending muscle weakness and areflexia from peripheral nerve involvement. In Guillain-Barré syndrome variants, however, some patients have unusual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8fb6257e06bdfcde914b4201e573bcd0
https://pubmed.ncbi.nlm.nih.gov/18365602
https://pubmed.ncbi.nlm.nih.gov/18365602
Publikováno v:
The Turkish journal of pediatrics. 49(4)
Subacute sclerosing panencephalitis (SSPE) usually begins insidiously and follows a subacute course with relentless but slow progression to death. In recent years, however, patients with acute or fulminant course were reported. In this article, we re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::61e8fe7be4a52db5cf9553a44bab76a4
https://pubmed.ncbi.nlm.nih.gov/18246746
https://pubmed.ncbi.nlm.nih.gov/18246746
Autor:
Banu, Anlar, Kader, Karli-Oğuz, Osman Yücel, Yurtyapan, Nesrin, Senbil, Ozlem, Hergüner, Sakir, Altunbaşak, F Müjgan, Sönmez, Pinar, Ozdemir-Geyik
Publikováno v:
The Turkish journal of pediatrics. 48(3)
Inherent abnormalities of myelin have been suggested in the pathogenesis of multiple sclerosis (MS). We investigated myelin in acute disseminated encephalomyelitis (ADEM) patients by magnetic resonance spectroscopy (MRS) and cerebrospinal fluid (CSF)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::466a81e5f114553db966cc89271d7dae
https://pubmed.ncbi.nlm.nih.gov/17172061
https://pubmed.ncbi.nlm.nih.gov/17172061