The associations among RARRES2
rs17173608 gene polymorphism, serum
chemerin, and non-traditional lipid profile
in patients with metabolic syndrome

Research Abstract
NULL
Research Authors
Marwa A. Dahpy1* , Marwa K. Khairallah2, Nashwa Mostafa A. Azoz2 and Ghada M. Ezzat1
Research Department
Department of Biochemistry
Research Journal
Egyptian Journal of Medical
Human Genetics
Research Member
Marwa Abdel Hafiz Abdel Aal Hassan
Research Pages
NULL
Research Publisher
springer
Research Rank
1
Research Vol
(2020) 21:21
Research Website
NULL
Research Year
2020

CLINICAL AND GENETIC ANALYSIS OF HEREDITARY PERIPHERAL NEUROPATHY IN EGYPTIAN POPULATION

Research Abstract
NULL
Research Authors
NA Haridy, Jana Vandrovcova, MA Abd El-Hamed, Sherifa Hamed, H Houlden
Research Department
Department of Neurology and Psychiatry
Research Journal
15th International Congress on Neuromuscular Diseases, July 6 - 10, 2018At: Vienna, Austria
Research Member
Nourelhoda Ahmed Ahmed Haridy
Research Pages
NULL
Research Publisher
NULL
Research Rank
1
Research Vol
NULL
Research Website
NULL
Research Year
2018

CLINICAL AND GENETIC ANALYSIS OF HEREDITARY PERIPHERAL NEUROPATHY IN EGYPTIAN POPULATION

Research Abstract
NULL
Research Authors
NA Haridy, Jana Vandrovcova, MA Abd El-Hamed, Sherifa Hamed, H Houlden
Research Department
Department of Neurology and Psychiatry
Research Journal
15th International Congress on Neuromuscular Diseases, July 6 - 10, 2018At: Vienna, Austria
Research Member
Mohamed Ahmed Abdel-Hamid Ibrahim
Research Pages
NULL
Research Publisher
NULL
Research Rank
1
Research Vol
NULL
Research Website
NULL
Research Year
2018

CLINICAL AND GENETIC ANALYSIS OF HEREDITARY PERIPHERAL NEUROPATHY IN EGYPTIAN POPULATION

Research Abstract
NULL
Research Authors
NA Haridy, Jana Vandrovcova, MA Abd El-Hamed, Sherifa Hamed, H Houlden
Research Department
Department of Neurology and Psychiatry
Research Journal
15th International Congress on Neuromuscular Diseases, July 6 - 10, 2018At: Vienna, Austria
Research Member
Sherifa Ahmed Hamed Omran
Research Pages
NULL
Research Publisher
NULL
Research Rank
1
Research Vol
NULL
Research Website
NULL
Research Year
2018

Clinical and Genetic analysis of Egyptian hereditary spastic paraplegia using next generation sequencing

Research Abstract
NULL
Research Authors
NA Haridy, V Chelban, J Vandrovcova, S Efthymiou, MA Abd El-Hamed, SA Hamed, H Houlden
Research Department
Department of Neurology and Psychiatry
Research Journal
Neuromuscular Disorders
Research Member
Nourelhoda Ahmed Ahmed Haridy
Research Pages
NULL
Research Publisher
Elsevier
Research Rank
1
Research Vol
28-S38
Research Website
NULL
Research Year
2018

Clinical and Genetic analysis of Egyptian hereditary spastic paraplegia using next generation sequencing

Research Abstract
NULL
Research Authors
NA Haridy, V Chelban, J Vandrovcova, S Efthymiou, MA Abd El-Hamed, SA Hamed, H Houlden
Research Department
Department of Neurology and Psychiatry
Research Journal
Neuromuscular Disorders
Research Member
Mohamed Ahmed Abdel-Hamid Ibrahim
Research Pages
NULL
Research Publisher
Elsevier
Research Rank
1
Research Vol
28-S38
Research Website
NULL
Research Year
2018

Clinical and Genetic analysis of Egyptian hereditary spastic paraplegia using next generation sequencing

Research Abstract
NULL
Research Authors
NA Haridy, V Chelban, J Vandrovcova, S Efthymiou, MA Abd El-Hamed, SA Hamed, H Houlden
Research Department
Department of Neurology and Psychiatry
Research Journal
Neuromuscular Disorders
Research Member
Sherifa Ahmed Hamed Omran
Research Pages
NULL
Research Publisher
Elsevier
Research Rank
1
Research Vol
28-S38
Research Website
NULL
Research Year
2018

Sequencing analysis of the SCA6 CAG expansion excludes an influence of repeat interruptions on disease onset

Research Abstract
NULL
Research Authors
Sarah Wiethoff, Emer O’Connor, Nourelhoda A Haridy, Suran Nethisinghe, Nicholas Wood, Paola Giunti, Conceição Bettencourt, Henry Houlden
Research Department
Department of Neurology and Psychiatry
Research Journal
Journal of Neurology, Neurosurgery & Psychiatry
Research Member
Nourelhoda Ahmed Ahmed Haridy
Research Pages
1226-1227
Research Publisher
BMJ Publishing Group Ltd
Research Rank
1
Research Vol
89-11
Research Website
NULL
Research Year
2018

Severe axonal neuropathy is a late manifestation of SPG11

Research Abstract
NULL
Research Authors
Andreea Manole, Viorica Chelban, Nourelhoda A Haridy, Sherifa A Hamed, Andrés Berardo, Mary M Reilly, Henry Houlden
Research Department
Department of Neurology and Psychiatry
Research Journal
Journal of neurology
Research Member
Nourelhoda Ahmed Ahmed Haridy
Research Pages
2278-2286
Research Publisher
Springer Berlin Heidelberg
Research Rank
1
Research Vol
263-11
Research Website
NULL
Research Year
2016

Severe axonal neuropathy is a late manifestation of SPG11

Research Abstract
NULL
Research Authors
Andreea Manole, Viorica Chelban, Nourelhoda A Haridy, Sherifa A Hamed, Andrés Berardo, Mary M Reilly, Henry Houlden
Research Department
Department of Neurology and Psychiatry
Research Journal
Journal of neurology
Research Member
Sherifa Ahmed Hamed Omran
Research Pages
2278-2286
Research Publisher
Springer Berlin Heidelberg
Research Rank
1
Research Vol
263-11
Research Website
NULL
Research Year
2016
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