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Göknur Haliloglu

Showing results (1-10 of 8) with videos related to

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Pediatric Transplantation|May 6, 2009
Pseudopapilledema in a pediatric kidney transplant recipientYelda Bilginer, Göknur Haliloglu, Sibel Kadayıfçılar, et al.
Neuromuscular Disorders : NMD|March 29, 2005
An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 geneBurcu Balci, Gökhan Uyanik, Pervin Dincer, et al.
European Journal of Pediatrics|January 18, 2006
Calpain-3 mutations in TurkeyBurcu Balci, Stefania Aurino, Göknur Haliloglu, et al.
Neuromuscular Disorders : NMD|December 18, 2003
A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of alpha-dystroglycanPervin Dinçer, Burcu Balci, Yeliz Yuva, et al.
Annals of Clinical and Translational Neurology|November 5, 2019
Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosisMarcel Naumann, Kevin Peikert, Rene Günther, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 5, 2019
The genomic and clinical landscape of fetal akinesiaMatthias Pergande, Susanne Motameny, Özkan Özdemir, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 27, 2020
Correction: The genomic and clinical landscape of fetal akinesiaMatthias Pergande, Susanne Motameny, Özkan Özdemir, et al.
Annals of Neurology|October 27, 2010
Early onset collagen VI myopathies: Genetic and clinical correlationsLaura Briñas, Pascale Richard, Susana Quijano-Roy, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Pediatric Transplantation|May 6, 2009
Pseudopapilledema in a pediatric kidney transplant recipientYelda Bilginer, Göknur Haliloglu, Sibel Kadayıfçılar, et al.
Neuromuscular Disorders : NMD|March 29, 2005
An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 geneBurcu Balci, Gökhan Uyanik, Pervin Dincer, et al.
European Journal of Pediatrics|January 18, 2006
Calpain-3 mutations in TurkeyBurcu Balci, Stefania Aurino, Göknur Haliloglu, et al.
Neuromuscular Disorders : NMD|December 18, 2003
A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of alpha-dystroglycanPervin Dinçer, Burcu Balci, Yeliz Yuva, et al.
Annals of Clinical and Translational Neurology|November 5, 2019
Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosisMarcel Naumann, Kevin Peikert, Rene Günther, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 5, 2019
The genomic and clinical landscape of fetal akinesiaMatthias Pergande, Susanne Motameny, Özkan Özdemir, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 27, 2020
Correction: The genomic and clinical landscape of fetal akinesiaMatthias Pergande, Susanne Motameny, Özkan Özdemir, et al.
Annals of Neurology|October 27, 2010
Early onset collagen VI myopathies: Genetic and clinical correlationsLaura Briñas, Pascale Richard, Susana Quijano-Roy, et al.
Pageof 1