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Changing Pattern of Fascioliasis Prevalence Early in the 3Rd Millennium in Dakahlia Governorate , Egypt: An Update

Journal of the Egyptian Society of Parasitology, 2013-04, Vol.43 (1), p.275-286

2013

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A novel point mutation of the androgen receptor (F804L) in an Egyptian newborn with complete androgen insensitivity associated with congenital glaucoma and hypertrophic pyloric stenosis

Clinical genetics, 2003-01, Vol.63 (1), p.59-63

2003

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The milder phenotype of the dystrophin gene double deletions

Acta neurologica Scandinavica, 2003-06, Vol.107 (6), p.400-404

2003

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A Novel Nonsense Mutation in Exon 1 of HSD17B3 Gene in an Egyptian 46,XY Adult Female Presenting with Primary Amenorrhea

Sexual development, 2013-01, Vol.7 (6), p.277-281

2013

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Detection of the G34R Mutation in the 5 Alpha Reductase 2 Gene by Allele Specific PCR and Its Linkage to the 89L Allele among Egyptian Cases

Sexual development, 2007-01, Vol.1 (5), p.293-296

2007

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Screening for six Mediterranean mutations in 90 Egyptian patients with phenylketonuria

Bratislavské lékarské listy, 2008, Vol.109 (1), p.17-19

2008

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Revisiting the harem conspiracy and death of Ramesses III: anthropological, forensic, radiological, and genetic study

BMJ (Online), 2012-12, Vol.345 (dec14 14), p.e8268-e8268

2012

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Molecular analysis of androgen resistance syndromes in Egyptian patients

Disease markers, 1997-04, Vol.13 (2), p.99-105

1997

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DIHYDROTESTOSTERONE REGULATES PLASMA SEX-HORMONE-BINDING GLOBULIN IN PREPUBERTAL MALES

Clinical endocrinology (Oxford), 1989-03, Vol.30 (3), p.279-284

1989

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Schistosoma hematobium soluble egg antigens induce proliferation of urothelial and endothelial cells

World journal of urology, 2001-08, Vol.19 (4), p.263-266

2001

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5α‐Reductase deficiency in patients with micropenis

Journal of inherited metabolic disease, 1997-03, Vol.20 (1), p.95-101

1997

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Studies of up-regulation of androgen receptors in genital skin fibroblasts

Molecular and cellular endocrinology, 1988-06, Vol.57 (3), p.205-213

1988

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5 alpha-reductase deficiency in patients with micropenis

Journal of inherited metabolic disease, 1997-03, Vol.20 (1), p.95-101

1997

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Familial Leydig cell hypoplasia as a cause of male pseudohermaphroditism

Human heredity, 1987-01, Vol.37 (1), p.36-40

1987

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Molecular analysis of 5α-reductase type 2 gene in eight unrelated egyptian children with suspected 5α-reductase deficiency: prevalence of the G34R mutation

Clinical endocrinology (Oxford), 2003-05, Vol.58 (5), p.627-631

2003

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A Novel Double Mutation in the Luteinizing Hormone Receptor in a Kindred with Familial Leydig Cell Hypoplasia and Male Pseudohermaphroditism

Endocrine research, 2005, Vol.31 (4), p.307-323

2005

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Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1

Molecular genetics & genomic medicine, 2021-12, Vol.9 (12), p.e1631-n/a

2021

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Insights from ancient DNA analysis of Egyptian human mummies: clues to disease and kinship

Human molecular genetics, 2021-04, Vol.30 (R1), p.R24-R28

2021

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Early role of vascular dysregulation on late-onset Alzheimer's disease based on multifactorial data-driven analysis

Nature communications, 2016-06, Vol.7 (1), p.11934-11934, Article 11934

2016

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An intronic DHCR7 genetic polymorphism associates with vitamin D serum level and incidence of acute coronary syndrome

Steroids, 2021-05, Vol.169, p.108825, Article 108825

2021

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A computational atlas of the hippocampal formation using ex vivo, ultra-high resolution MRI: Application to adaptive segmentation of in vivo MRI

NeuroImage (Orlando, Fla.), 2015-07, Vol.115, p.117-137

2015

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Predicting Alzheimer's disease progression using multi-modal deep learning approach

Scientific reports, 2019-02, Vol.9 (1), p.1952, Article 1952

2019

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Machine learning framework for early MRI-based Alzheimer's conversion prediction in MCI subjects

NeuroImage (Orlando, Fla.), 2015-01, Vol.104, p.398-412

2015

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Developing a Road Map to Spread Genomic Knowledge in Africa: 10th Conference of the African Society of Human Genetics, Cairo, Egypt

The American journal of tropical medicine and hygiene, 2020-04, Vol.102 (4), p.719-723

2020

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Characterizing Heterogeneity in Neuroimaging, Cognition, Clinical Symptoms, and Genetics Among Patients With Late-Life Depression

JAMA psychiatry (Chicago, Ill.), 2022-05, Vol.79 (5), p.464

2022

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Changing Pattern of Fascioliasis Prevalence Early in the 3Rd Millennium in Dakahlia Governorate , Egypt: An Update

A novel point mutation of the androgen receptor (F804L) in an Egyptian newborn with complete androgen insensitivity associated with congenital glaucoma and hypertrophic pyloric stenosis

The milder phenotype of the dystrophin gene double deletions

A Novel Nonsense Mutation in Exon 1 of HSD17B3 Gene in an Egyptian 46,XY Adult Female Presenting with Primary Amenorrhea

Detection of the G34R Mutation in the 5 Alpha Reductase 2 Gene by Allele Specific PCR and Its Linkage to the 89L Allele among Egyptian Cases

Screening for six Mediterranean mutations in 90 Egyptian patients with phenylketonuria

Revisiting the harem conspiracy and death of Ramesses III: anthropological, forensic, radiological, and genetic study

Molecular analysis of androgen resistance syndromes in Egyptian patients

DIHYDROTESTOSTERONE REGULATES PLASMA SEX-HORMONE-BINDING GLOBULIN IN PREPUBERTAL MALES

Schistosoma hematobium soluble egg antigens induce proliferation of urothelial and endothelial cells

5α‐Reductase deficiency in patients with micropenis

Studies of up-regulation of androgen receptors in genital skin fibroblasts

5 alpha-reductase deficiency in patients with micropenis

Familial Leydig cell hypoplasia as a cause of male pseudohermaphroditism

Molecular analysis of 5α-reductase type 2 gene in eight unrelated egyptian children with suspected 5α-reductase deficiency: prevalence of the G34R mutation

A Novel Double Mutation in the Luteinizing Hormone Receptor in a Kindred with Familial Leydig Cell Hypoplasia and Male Pseudohermaphroditism

Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1

Insights from ancient DNA analysis of Egyptian human mummies: clues to disease and kinship

Early role of vascular dysregulation on late-onset Alzheimer's disease based on multifactorial data-driven analysis

An intronic DHCR7 genetic polymorphism associates with vitamin D serum level and incidence of acute coronary syndrome

A computational atlas of the hippocampal formation using ex vivo, ultra-high resolution MRI: Application to adaptive segmentation of in vivo MRI

Predicting Alzheimer's disease progression using multi-modal deep learning approach

Machine learning framework for early MRI-based Alzheimer's conversion prediction in MCI subjects

Developing a Road Map to Spread Genomic Knowledge in Africa: 10th Conference of the African Society of Human Genetics, Cairo, Egypt

Characterizing Heterogeneity in Neuroimaging, Cognition, Clinical Symptoms, and Genetics Among Patients With Late-Life Depression

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