Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H Topaloglu

Showing results (21-30 of 69) with videos related to

Pageof 7
Sort By:
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 1, 1997
Intravenous immunoglobulin treatment in children with Guillain-Barré syndromeG Kanra, A Ozon, J Vajsar, et al.
American Journal of Hematology|November 26, 1997
Cerebral infarct associated with factor V Leiden mutation in a boy with hemophilia AL Olcay, A Gürgey, H Topaloglu, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 4, 2000
Clinical and histopathological study of merosin-deficient and merosin-positive congenital muscular dystrophyB Talim, G Kale, H Topaloglu, et al.
Neuropediatrics|July 13, 1999
Clinical and genetic correlate in childhood onset Friedreich ataxiaM Alikaşifoglu, H Topaloglu, E Tunçbilek, et al.
Eye (London, England)|May 8, 2001
Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy populationC F Dogulu, T Kansu, V Seyrantepe, et al.
Urologia Internationalis|November 14, 2012
Lymphangioma of pyeloureteral junction: an extremely rare caseH Topaloglu, N Karakoyunlu, U Ozok, et al.
Human Genetics|September 10, 1999
The human CDC42 gene: genomic organization, evidence for the existence of a putative pseudogene and exclusion as a SJS1 candidate geneS Nicole, P S White, H Topaloglu, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|June 9, 2005
Clinical spectrum of muscle-eye-brain disease: from the typical presentation to severe autistic featuresG Haliloglu, C Gross, N Senbil, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Prenatal diagnosis in merosin-deficient congenital muscular dystrophyI Naom, C Sewry, M D'Alessandro, et al.
Scottish Medical Journal|April 19, 2013
Evaluation of erectile dysfunction in permanent pacemaker implanted patients with cardiac rhythm disorder prediagnosisL Sagnak, H Ersoy, N Karakoyunlu, et al.
Pageof 7

Showing results (21-30 of 69) with videos related to

Sort By:
Pageof 7
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 1, 1997
Intravenous immunoglobulin treatment in children with Guillain-Barré syndromeG Kanra, A Ozon, J Vajsar, et al.
American Journal of Hematology|November 26, 1997
Cerebral infarct associated with factor V Leiden mutation in a boy with hemophilia AL Olcay, A Gürgey, H Topaloglu, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 4, 2000
Clinical and histopathological study of merosin-deficient and merosin-positive congenital muscular dystrophyB Talim, G Kale, H Topaloglu, et al.
Neuropediatrics|July 13, 1999
Clinical and genetic correlate in childhood onset Friedreich ataxiaM Alikaşifoglu, H Topaloglu, E Tunçbilek, et al.
Eye (London, England)|May 8, 2001
Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy populationC F Dogulu, T Kansu, V Seyrantepe, et al.
Urologia Internationalis|November 14, 2012
Lymphangioma of pyeloureteral junction: an extremely rare caseH Topaloglu, N Karakoyunlu, U Ozok, et al.
Human Genetics|September 10, 1999
The human CDC42 gene: genomic organization, evidence for the existence of a putative pseudogene and exclusion as a SJS1 candidate geneS Nicole, P S White, H Topaloglu, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|June 9, 2005
Clinical spectrum of muscle-eye-brain disease: from the typical presentation to severe autistic featuresG Haliloglu, C Gross, N Senbil, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Prenatal diagnosis in merosin-deficient congenital muscular dystrophyI Naom, C Sewry, M D'Alessandro, et al.
Scottish Medical Journal|April 19, 2013
Evaluation of erectile dysfunction in permanent pacemaker implanted patients with cardiac rhythm disorder prediagnosisL Sagnak, H Ersoy, N Karakoyunlu, et al.
Pageof 7