Search research articles
Contact Us
Filters
Showing results (1-10 of 58) with videos related to
Page
of 6
Sort By:
Neuromuscular Disorders : NMD
|
February 13, 2019
Neuromuscular disorders in Anatolia - A personal review
Haluk Topaloğlu
Developmental Medicine and Child Neurology
|
September 6, 2022
The complex genetic inheritance of Anatolia, Turkey
Haluk Topaloğlu
Neuromuscular Disorders : NMD
|
February 27, 2019
Fractures and bone health in Duchenne muscular dystrophy in Scotland
Haluk Topaloğlu
Handbook of Clinical Neurology
|
September 24, 2008
Lissencephaly type II
Haluk Topaloğlu, Beril Talim
Genes
|
July 27, 2022
Current Outline of Exon Skipping Trials in Duchenne Muscular Dystrophy
Gökçe Eser, Haluk Topaloğlu
Current Opinion in Neurology
|
September 16, 2004
Glycosylation defects in muscular dystrophies
Göknur Haliloğlu, Haluk Topaloğlu
Neuromuscular Disorders : NMD
|
November 2, 2023
Smartphone measures motor and respiratory function in spinal muscular atrophy
Haluk Topaloğlu, Ayşe Nur Coşkun
The Turkish Journal of Pediatrics
|
June 2, 2009
An unusual presentation of gastrointestinal obstruction in a three-year-old boy
Ozlem Boybeyi, Arbay Ozden Ciftçi, Haluk Topaloğlu
Neuropediatrics
|
November 20, 2018
Diagnostic Pathway to Nonsense Mutation Dystrophinopathy: A Tertiary-Center, Retrospective Experience
Didem Ardıçlı, Goknur Haliloğlu, Mehmet Alikaşifoğlu, et al.
Advances in Therapy
|
March 18, 2008
A preliminary report on spinal muscular atrophy lymphoblastoid cell lines: are they an appropriate tool for drug screening?
Didem Dayangaç-Erden, Haluk Topaloğlu, Hayat Erdem-Yurter
Page
of 6
Search research articles
Search
Showing results (1-10 of 58) with videos related to
Sort By:
Page
of 6
Neuromuscular Disorders : NMD
|
February 13, 2019
Neuromuscular disorders in Anatolia - A personal review
Haluk Topaloğlu
Developmental Medicine and Child Neurology
|
September 6, 2022
The complex genetic inheritance of Anatolia, Turkey
Haluk Topaloğlu
Neuromuscular Disorders : NMD
|
February 27, 2019
Fractures and bone health in Duchenne muscular dystrophy in Scotland
Haluk Topaloğlu
Handbook of Clinical Neurology
|
September 24, 2008
Lissencephaly type II
Haluk Topaloğlu, Beril Talim
Genes
|
July 27, 2022
Current Outline of Exon Skipping Trials in Duchenne Muscular Dystrophy
Gökçe Eser, Haluk Topaloğlu
Current Opinion in Neurology
|
September 16, 2004
Glycosylation defects in muscular dystrophies
Göknur Haliloğlu, Haluk Topaloğlu
Neuromuscular Disorders : NMD
|
November 2, 2023
Smartphone measures motor and respiratory function in spinal muscular atrophy
Haluk Topaloğlu, Ayşe Nur Coşkun
The Turkish Journal of Pediatrics
|
June 2, 2009
An unusual presentation of gastrointestinal obstruction in a three-year-old boy
Ozlem Boybeyi, Arbay Ozden Ciftçi, Haluk Topaloğlu
Neuropediatrics
|
November 20, 2018
Diagnostic Pathway to Nonsense Mutation Dystrophinopathy: A Tertiary-Center, Retrospective Experience
Didem Ardıçlı, Goknur Haliloğlu, Mehmet Alikaşifoğlu, et al.
Advances in Therapy
|
March 18, 2008
A preliminary report on spinal muscular atrophy lymphoblastoid cell lines: are they an appropriate tool for drug screening?
Didem Dayangaç-Erden, Haluk Topaloğlu, Hayat Erdem-Yurter
Page
of 6