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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 syndrome
G 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 A
L 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 dystrophy
B Talim, G Kale, H Topaloglu, et al.
Neuropediatrics
|
July 13, 1999
Clinical and genetic correlate in childhood onset Friedreich ataxia
M Alikaşifoglu, H Topaloglu, E Tunçbilek, et al.
Eye (London, England)
|
May 8, 2001
Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population
C F Dogulu, T Kansu, V Seyrantepe, et al.
Urologia Internationalis
|
November 14, 2012
Lymphangioma of pyeloureteral junction: an extremely rare case
H 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 gene
S 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 features
G Haliloglu, C Gross, N Senbil, et al.
Neuromuscular Disorders : NMD
|
May 1, 1997
Prenatal diagnosis in merosin-deficient congenital muscular dystrophy
I 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 prediagnosis
L Sagnak, H Ersoy, N Karakoyunlu, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 69) with videos related to
Sort By:
Page
of 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 syndrome
G 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 A
L 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 dystrophy
B Talim, G Kale, H Topaloglu, et al.
Neuropediatrics
|
July 13, 1999
Clinical and genetic correlate in childhood onset Friedreich ataxia
M Alikaşifoglu, H Topaloglu, E Tunçbilek, et al.
Eye (London, England)
|
May 8, 2001
Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population
C F Dogulu, T Kansu, V Seyrantepe, et al.
Urologia Internationalis
|
November 14, 2012
Lymphangioma of pyeloureteral junction: an extremely rare case
H 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 gene
S 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 features
G Haliloglu, C Gross, N Senbil, et al.
Neuromuscular Disorders : NMD
|
May 1, 1997
Prenatal diagnosis in merosin-deficient congenital muscular dystrophy
I 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 prediagnosis
L Sagnak, H Ersoy, N Karakoyunlu, et al.
Page
of 7