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P Serdaroglu

Showing results (11-20 of 19) with videos related to

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Clinical Genetics|January 5, 2001
Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type 1 and HNPP patientsN Bissar-Tadmouri, Y Parman, L Boutrand, et al.
European Journal of Neurology|January 11, 2002
Cerebral vasculitis and ischaemic stroke in Behçet's disease: report of one case and review of the literatureY Krespi, G Akman-Demir, M Poyraz, et al.
Journal of Neurology|October 13, 2001
The range of chronic demyelinating neuropathy of infancy: a clinico-pathological and genetic study of 15 unrelated casesV Planté-Bordeneuve, Y Parman, A Guiochon-Mantel, et al.
Archives of Neurology|July 1, 1996
Seven-year follow-up of neurologic involvement in Behçet syndromeG Akman-Demir, B Baykan-Kurt, P Serdaroglu, et al.
Neurology|February 21, 2007
Clinical comparison of anti-MuSK- vs anti-AChR-positive and seronegative myasthenia gravisF Deymeer, O Gungor-Tuncer, V Yilmaz, et al.
Neurology|May 12, 2004
Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second geneN Bissar-Tadmouri, E Nelis, S Züchner, et al.
Human Molecular Genetics|April 1, 1997
Mapping of the familial infantile myasthenia (congenital myasthenic syndrome type Ia) gene to chromosome 17p with evidence of genetic homogeneityK Christodoulou, M Tsingis, F Deymeer, et al.
Neurology|January 19, 2011
Oculopharyngodistal myopathy is a distinct entity: clinical and genetic features of 47 patientsH Durmus, S H Laval, F Deymeer, et al.
Cell|May 24, 2001
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndromeN M Plaster, R Tawil, M Tristani-Firouzi, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Clinical Genetics|January 5, 2001
Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type 1 and HNPP patientsN Bissar-Tadmouri, Y Parman, L Boutrand, et al.
European Journal of Neurology|January 11, 2002
Cerebral vasculitis and ischaemic stroke in Behçet's disease: report of one case and review of the literatureY Krespi, G Akman-Demir, M Poyraz, et al.
Journal of Neurology|October 13, 2001
The range of chronic demyelinating neuropathy of infancy: a clinico-pathological and genetic study of 15 unrelated casesV Planté-Bordeneuve, Y Parman, A Guiochon-Mantel, et al.
Archives of Neurology|July 1, 1996
Seven-year follow-up of neurologic involvement in Behçet syndromeG Akman-Demir, B Baykan-Kurt, P Serdaroglu, et al.
Neurology|February 21, 2007
Clinical comparison of anti-MuSK- vs anti-AChR-positive and seronegative myasthenia gravisF Deymeer, O Gungor-Tuncer, V Yilmaz, et al.
Neurology|May 12, 2004
Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second geneN Bissar-Tadmouri, E Nelis, S Züchner, et al.
Human Molecular Genetics|April 1, 1997
Mapping of the familial infantile myasthenia (congenital myasthenic syndrome type Ia) gene to chromosome 17p with evidence of genetic homogeneityK Christodoulou, M Tsingis, F Deymeer, et al.
Neurology|January 19, 2011
Oculopharyngodistal myopathy is a distinct entity: clinical and genetic features of 47 patientsH Durmus, S H Laval, F Deymeer, et al.
Cell|May 24, 2001
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndromeN M Plaster, R Tawil, M Tristani-Firouzi, et al.
Pageof 2