Nagia Fahmy

About Nagia Fahmy

Nagia Fahmy, With an exceptional h-index of 7 and a recent h-index of 7 (since 2020), a distinguished researcher at Ain Shams University, specializes in the field of Neurology, Neuromuscular, Genetics, Molecular Biology.

His recent articles reflect a diverse array of research interests and contributions to the field:

Familial amyotrophic lateral sclerosis and multiple sclerosis in an Egyptian family. A family report

Egyptian adaptation and validation of the Edinburgh Cognitive and Behavioral Amyotrophic Lateral Sclerosis Screen (ECAS-EG)

A novel homozygous p.Ser69Pro SOD1 mutation causes severe young-onset ALS with decreased enzyme activity

MicroRNAs as a Tool for Differential Diagnosis of Neuromuscular Disorders

MLPA analysis for molecular diagnosis of spinal muscular atrophy and correlation of 5q13. 2 genes with disease phenotype in Egyptian patients

Cognitive and neurobehavioral patterns in a sample of Egyptian patients genetically diagnosed with Duchenne muscular dystrophy

SERUM LEVEL OF RETINOL BINDING PROTEIN 4 IN RELATION TO AMYOTROPHIC LATERAL SCLEROSIS AMONG EGYPTIAN PATIENTS

Case Report: A Novel AChR Epsilon Variant Causing a Clinically Discordant Salbutamol Responsive Congenital Myasthenic Syndrome in Two Egyptian Siblings

Nagia Fahmy Information

University

Position

Professor of Neurology Faculty of Medicine

Citations(all)

204

Citations(since 2020)

185

Cited By

56

hIndex(all)

7

hIndex(since 2020)

7

i10Index(all)

5

i10Index(since 2020)

3

Email

University Profile Page

Google Scholar

Nagia Fahmy Skills & Research Interests

Neurology

Neuromuscular

Genetics

Molecular Biology

Top articles of Nagia Fahmy

Familial amyotrophic lateral sclerosis and multiple sclerosis in an Egyptian family. A family report

Brain Disorders

2023/9/1

Nagia Fahmy
Nagia Fahmy

H-Index: 4

Egyptian adaptation and validation of the Edinburgh Cognitive and Behavioral Amyotrophic Lateral Sclerosis Screen (ECAS-EG)

2023/6

Ahmad Osman
Ahmad Osman

H-Index: 0

Nagia Fahmy
Nagia Fahmy

H-Index: 4

A novel homozygous p.Ser69Pro SOD1 mutation causes severe young-onset ALS with decreased enzyme activity

Journal of Neurology

2023/3

Nagia Fahmy
Nagia Fahmy

H-Index: 4

Kathrin Müller
Kathrin Müller

H-Index: 6

MicroRNAs as a Tool for Differential Diagnosis of Neuromuscular Disorders

NeuroMolecular Medicine

2023/12

MLPA analysis for molecular diagnosis of spinal muscular atrophy and correlation of 5q13. 2 genes with disease phenotype in Egyptian patients

Egyptian Journal of Medical Human Genetics

2022/12/5

Cognitive and neurobehavioral patterns in a sample of Egyptian patients genetically diagnosed with Duchenne muscular dystrophy

Middle East Current Psychiatry

2022/10/6

SERUM LEVEL OF RETINOL BINDING PROTEIN 4 IN RELATION TO AMYOTROPHIC LATERAL SCLEROSIS AMONG EGYPTIAN PATIENTS

Ain Shams Medical Journal

2022/9/1

Randa Reda
Randa Reda

H-Index: 2

Nagia Fahmy
Nagia Fahmy

H-Index: 4

Case Report: A Novel AChR Epsilon Variant Causing a Clinically Discordant Salbutamol Responsive Congenital Myasthenic Syndrome in Two Egyptian Siblings

Frontiers in neurology

2022/6/2

Nagia Fahmy
Nagia Fahmy

H-Index: 4

Ambulatory Duchenne muscular dystrophy children: Cross-sectional correlation between function, quantitative muscle ultrasound and MRI

Acta Myologica

2022/3

Nagia Fahmy
Nagia Fahmy

H-Index: 4

Heba Elsedfy
Heba Elsedfy

H-Index: 15

Validity of skeletal muscle ultrasound as a screening tool in the assessment of patients with suspected limb-girdle muscular dystrophy

Journal of Clinical Neuroscience

2022/2/1

Role of neuro-sonography of peripheral nerves as a diagnostic and a differentiation tool of amyotrophic lateral sclerosis

The Egyptian Journal of Neurology, Psychiatry and Neurosurgery

2021/12

Global longitudinal strain detects subtle left ventricular systolic dysfunction in Duchenne muscular dystrophy patients and carriers

The Egyptian Heart Journal

2021/12

VALUE OF MUSCLE MAGNETIC RESONANCE IMAGING IN COMPARISON WITH MUSCLE BIOPSY FOR DIFFERENTIATING VARIOUS TYPES OF LGMD

QJM: An International Journal of Medicine

2021/10/1

Validity of Skeletal Muscle Ultrasound in Assessment of Suspected Limb Girdle Muscular Dystrophy Patients

QJM: An International Journal of Medicine

2021/10/1

MOTOR NEURON DISORDERS AND NEUROPATHIES: EP. 243 Young-onset SOD1-ALS caused by a novel homozygous mutation, a family report

Neuromuscular Disorders

2021/10/1

Hossam M Shokri, MD, PhD, Magd Zakaria, MD, PhD, Hany Aref, MD, PhD, Nagia Fahmi, MD, PhD, Naglaa Khayat, MD, PhD, Ali Shalash, MD, PhD, and

JOURNAL OF STROKE & CEREBROVASCULAR DISEASES

2021/9/1

miRNome profiling in Duchenne muscular dystrophy; identification of asymptomatic and manifesting female carriers

Bioscience Reports

2021/9

Assessment of diagnostic potential of some circulating microRNAs in amyotrophic lateral sclerosis patients, an Egyptian study

Clinical Neurology and Neurosurgery

2021/9/1

Ahmad Osman
Ahmad Osman

H-Index: 0

Nagia Fahmy
Nagia Fahmy

H-Index: 4

Whole-body muscle MRI characteristics of LAMA2-related congenital muscular dystrophy children: an emerging pattern

Neuromuscular Disorders

2021/9/1

Nagia Fahmy
Nagia Fahmy

H-Index: 4

The clinical characteristics of patients with pre-existing leukoaraiosis compared to those without leukoaraiosis in acute ischemic stroke

Journal of Stroke and Cerebrovascular Diseases

2021/9/1

See List of Professors in Nagia Fahmy University(Ain Shams University)

Co-Authors

academic-engine