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Beril Talim

Showing results (51-60 of 118) with videos related to

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Indian Journal of Pediatrics|August 17, 2013
Vesiculopustular eruption in neonatal transient myeloproliferative disorderIraz Nar, Ozge Surmeli-Onay, Selin Aytac, et al.
Iranian Journal of Radiology : a Quarterly Journal Published by the Iranian Radiological Society|November 18, 2016
Giant Omental Cyst (Lymphangioma) Mimicking Ascites and TuberculosisAsuman Nur Karhan, Tutku Soyer, Altan Gunes, et al.
The Turkish Journal of Pediatrics|November 7, 2013
Serum alpha-fetoprotein levels in neonatal cholestasisHülya Demir, Gülin Hızal, Nuray Uslu Kızılkan, et al.
Neuromuscular Disorders : NMD|August 15, 2009
An unusual presentation of muscle-eye-brain disease: severe eye abnormalities with mild muscle and brain involvementErcan Demir, Kivilcim Gucuyener, Aysima Akturk, et al.
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.
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.
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.
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.
Pageof 12

Showing results (51-60 of 118) with videos related to

Sort By:
Pageof 12
Indian Journal of Pediatrics|August 17, 2013
Vesiculopustular eruption in neonatal transient myeloproliferative disorderIraz Nar, Ozge Surmeli-Onay, Selin Aytac, et al.
Iranian Journal of Radiology : a Quarterly Journal Published by the Iranian Radiological Society|November 18, 2016
Giant Omental Cyst (Lymphangioma) Mimicking Ascites and TuberculosisAsuman Nur Karhan, Tutku Soyer, Altan Gunes, et al.
The Turkish Journal of Pediatrics|November 7, 2013
Serum alpha-fetoprotein levels in neonatal cholestasisHülya Demir, Gülin Hızal, Nuray Uslu Kızılkan, et al.
Neuromuscular Disorders : NMD|August 15, 2009
An unusual presentation of muscle-eye-brain disease: severe eye abnormalities with mild muscle and brain involvementErcan Demir, Kivilcim Gucuyener, Aysima Akturk, et al.
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.
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.
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.
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.
Pageof 12