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Talim

Showing results (81-90 of 159) with videos related to

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The Turkish Journal of Pediatrics|December 30, 2022
Significance of intestinal alkaline phosphatase in predicting histological activity of pediatric inflammatory bowel diseaseBurcu Berberoğlu Ateş, Beril Talim, Hayriye Hizarcıoğlu Gülşen, et al.
Multiple Sclerosis and Related Disorders|January 3, 2018
Myelitis and cauda equina involvement following dengue fever. A case report and review of the literatureMarco A Lana-Peixoto, Denison Pedrosa, Natália Talim, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 16, 2006
Prenatal period to adolescence: the variable presentations of congenital cystic adenomatoid malformationAyse Tana Aslan, Ebru Yalcin, Tutku Soyer, et al.
Arquivos De Neuro-Psiquiatria|August 8, 2014
Sjögren syndrome and neuromyelitis optica spectrum disorder co-exist in a common autoimmune milieuDiogo C Carvalho, Tauana S Tironi, Denise S Freitas, et al.
Journal of Neuromuscular Diseases|March 31, 2015
Whole Exome Sequencing Reveals <i>DYSF</i>, <i>FKTN</i>, and <i>ISPD</i> Mutations in Congenital Muscular Dystrophy Without Brain or Eye InvolvementOzge Ceyhan-Birsoy, Beril Talim, Lindsay C Swanson, et al.
American Journal of Human Genetics|November 27, 2010
Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophyHulya Gundesli, Beril Talim, Petek Korkusuz, et al.
Klinische Padiatrie|March 7, 2022
A Rare Pediatric Case of Severe Rhabdomyolysis Owing to Dual InfectionÖzben Akıncı Göktaş, Ömer Bektaş, Gökçen Öz Tunçer, et al.
Journal of the Neurological Sciences|March 23, 2016
Hypovitaminosis D association with disease activity in relapsing remitting multiple sclerosis in BrazilJefferson Becker, Dagoberto Callegaro, Marco Aurélio Lana-Peixoto, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1)Eugenio Mercuri, Beril Talim, Behzad Moghadaszadeh, et al.
Clinical Genetics|August 10, 2025
A Founder Allele in SGCG Combining Missense Variant and Multi-Exon Duplication in Turkish Patients With SarcoglycanopathyAbdullah Sezer, Afife Büke, Hasan Hüseyin Kazan, et al.
Pageof 16

Showing results (81-90 of 159) with videos related to

Sort By:
Pageof 16
The Turkish Journal of Pediatrics|December 30, 2022
Significance of intestinal alkaline phosphatase in predicting histological activity of pediatric inflammatory bowel diseaseBurcu Berberoğlu Ateş, Beril Talim, Hayriye Hizarcıoğlu Gülşen, et al.
Multiple Sclerosis and Related Disorders|January 3, 2018
Myelitis and cauda equina involvement following dengue fever. A case report and review of the literatureMarco A Lana-Peixoto, Denison Pedrosa, Natália Talim, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 16, 2006
Prenatal period to adolescence: the variable presentations of congenital cystic adenomatoid malformationAyse Tana Aslan, Ebru Yalcin, Tutku Soyer, et al.
Arquivos De Neuro-Psiquiatria|August 8, 2014
Sjögren syndrome and neuromyelitis optica spectrum disorder co-exist in a common autoimmune milieuDiogo C Carvalho, Tauana S Tironi, Denise S Freitas, et al.
Journal of Neuromuscular Diseases|March 31, 2015
Whole Exome Sequencing Reveals <i>DYSF</i>, <i>FKTN</i>, and <i>ISPD</i> Mutations in Congenital Muscular Dystrophy Without Brain or Eye InvolvementOzge Ceyhan-Birsoy, Beril Talim, Lindsay C Swanson, et al.
American Journal of Human Genetics|November 27, 2010
Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophyHulya Gundesli, Beril Talim, Petek Korkusuz, et al.
Klinische Padiatrie|March 7, 2022
A Rare Pediatric Case of Severe Rhabdomyolysis Owing to Dual InfectionÖzben Akıncı Göktaş, Ömer Bektaş, Gökçen Öz Tunçer, et al.
Journal of the Neurological Sciences|March 23, 2016
Hypovitaminosis D association with disease activity in relapsing remitting multiple sclerosis in BrazilJefferson Becker, Dagoberto Callegaro, Marco Aurélio Lana-Peixoto, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1)Eugenio Mercuri, Beril Talim, Behzad Moghadaszadeh, et al.
Clinical Genetics|August 10, 2025
A Founder Allele in SGCG Combining Missense Variant and Multi-Exon Duplication in Turkish Patients With SarcoglycanopathyAbdullah Sezer, Afife Büke, Hasan Hüseyin Kazan, et al.
Pageof 16