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Novel Genomic Variants, Atypical Phenotypes and Evidence of a Digenic/Oligogenic Contribution to Disorders/Differences of Sex Development in a Large North African Cohort

Frontiers in genetics, 2022-08, Vol.13, p.900574-900574

2022

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A Genomic Screen of Autism: Evidence for a Multilocus Etiology

American journal of human genetics, 1999-08, Vol.65 (2), p.493-507

1999

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Abstract #1604725: COVID-19 Vaccination Hesitancy and Infection Patterns Among Thyroid Cancer Survivors: A Cross-Sectional Study

Endocrine practice, 2023-12, Vol.29 (12), p.S185

2023

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Abstract #1604735: Prevalence of Overweight, Obesity, and Android Obesity in Thyroid Cancer Survivors and Associated Factors

Endocrine practice, 2023-12, Vol.29 (12), p.S185-S186

2023

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Fréquence et caractéristiques cliniques et polygraphiques du SAHOS chez une population d’acromégales

Médecine du sommeil, 2024-03, Vol.21 (1), p.44-45

2024

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Management of patients with diabetes and obesity in the COVID-19 era: Experiences and learnings from South and East Europe, the Middle East, and Africa

Diabetes research and clinical practice, 2021-02, Vol.172, p.108617-108617, Article 108617

2021

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Fréquence de l’hypoglycémie chez les patients diabétiques de type 2 traités par insuline basale en Algérie (Hypo Study)

Médecine des maladies métaboliques, 2022-06, Vol.16 (4), p.351-358

2022

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AACE2021-A-1098: Clinical and Pathological Characteristics of Thyroid Cancer in Adolescents and Young Adults (AYA): An Algerian Observation

Endocrine practice, 2021-12, Vol.27 (12), p.S31-S31

2021

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Abstract #991725: Lack of Pathology Data as a Source of Misclassification of Thyroid Microcarcinoma Risk: An Algerian Observation

Endocrine practice, 2021-06, Vol.27 (6), p.S143-S144

2021

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Abstract #1325282: COVID-19 Vaccination Refusal Among Medullary Thyroid Cancer Survivors

Endocrine practice, 2022-12, Vol.28 (12), p.S70-S71

2022

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Évaluation de la performance clinique et analytique du système de mesure de glycémie Vital Check® MM-1200/bandelettes MS-2 dans la vraie vie

Médecine des maladies métaboliques, 2023-10, Vol.17 (6), p.507-516

2023

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CA-009 - Évaluation des activités enzymatiques antioxydantes érythrocytaires chez les diabétiques de type 2 souffrant d’une néphropathie

Diabetes & metabolism, 2017-03, Vol.43 (2), p.A53-A53

2017

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Évaluation des activités enzymatiques antioxydantes érythrocytaires chez les diabétiques de type 2 souffrant d’une néphropathie

Diabetes & metabolism, 2017-03, Vol.43 (2), p.A53

2017

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Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease

Nature genetics, 2002-10, Vol.32 (2), p.237-244

2002

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A Locus for Axonal Motor-Sensory Neuropathy with Deafness and Mental Retardation Maps to Xq24–q26

Genomics (San Diego, Calif.), 1995-09, Vol.29 (2), p.409-412

1995

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Linkage Mapping of the Human Thromboxane A2 Receptor (TBXA2R) to Chromosome 19p13.3 Using Transcribed 3′ Untranslated DNA Sequence Polymorphisms

Genomics (San Diego, Calif.), 1993-11, Vol.18 (2), p.212-215

1993

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Exclusion of linkage to the HLA region in ninety multiplex sibships with autism

Journal of autism and developmental disorders, 1999-06, Vol.29 (3), p.195-201

1999

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Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome II

American journal of human genetics, 1994-04, Vol.54 (4), p.681-686

1994

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A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10

Nature genetics, 1994-06, Vol.7 (2), p.149-153

1994

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Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11

American journal of human genetics, 1994-04, Vol.54 (4), p.681-686

1994

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Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism

American journal of medical genetics, 1999-10, Vol.88 (5), p.551-556

1999

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Comparative studies of the CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene

American journal of medical genetics, 1997-09, Vol.74 (5), p.488-493

1997

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Single‐Nucleotide Polymorphism Genotyping Using Microarrays

Current Protocols in Human Genetics, 2001-05, Vol.27 (1), p.2.9.1-2.9.16

2001

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Analysis of CAG repeat of the Machado-Joseph gene in human, chimpanzee and monkey populations : a variant nucleoside is associated with the number of CAG repeats

Human molecular genetics, 1996, Vol.5 (2), p.207-213

1996

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Pleiotropic Changes in Cycloheximideresistant Insect Cell Clones

In vitro cellular & developmental biology, 1987-03, Vol.23 (3), p.175-180

1987

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Novel Genomic Variants, Atypical Phenotypes and Evidence of a Digenic/Oligogenic Contribution to Disorders/Differences of Sex Development in a Large North African Cohort

A Genomic Screen of Autism: Evidence for a Multilocus Etiology

Abstract #1604725: COVID-19 Vaccination Hesitancy and Infection Patterns Among Thyroid Cancer Survivors: A Cross-Sectional Study

Abstract #1604735: Prevalence of Overweight, Obesity, and Android Obesity in Thyroid Cancer Survivors and Associated Factors

Fréquence et caractéristiques cliniques et polygraphiques du SAHOS chez une population d’acromégales

Management of patients with diabetes and obesity in the COVID-19 era: Experiences and learnings from South and East Europe, the Middle East, and Africa

Fréquence de l’hypoglycémie chez les patients diabétiques de type 2 traités par insuline basale en Algérie (Hypo Study)

AACE2021-A-1098: Clinical and Pathological Characteristics of Thyroid Cancer in Adolescents and Young Adults (AYA): An Algerian Observation

Abstract #991725: Lack of Pathology Data as a Source of Misclassification of Thyroid Microcarcinoma Risk: An Algerian Observation

Abstract #1325282: COVID-19 Vaccination Refusal Among Medullary Thyroid Cancer Survivors

Évaluation de la performance clinique et analytique du système de mesure de glycémie Vital Check® MM-1200/bandelettes MS-2 dans la vraie vie

CA-009 - Évaluation des activités enzymatiques antioxydantes érythrocytaires chez les diabétiques de type 2 souffrant d’une néphropathie

Évaluation des activités enzymatiques antioxydantes érythrocytaires chez les diabétiques de type 2 souffrant d’une néphropathie

Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease

A Locus for Axonal Motor-Sensory Neuropathy with Deafness and Mental Retardation Maps to Xq24–q26

Linkage Mapping of the Human Thromboxane A2 Receptor (TBXA2R) to Chromosome 19p13.3 Using Transcribed 3′ Untranslated DNA Sequence Polymorphisms

Exclusion of linkage to the HLA region in ninety multiplex sibships with autism

Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome II

A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10

Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11

Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism

Comparative studies of the CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene

Single‐Nucleotide Polymorphism Genotyping Using Microarrays

Analysis of CAG repeat of the Machado-Joseph gene in human, chimpanzee and monkey populations : a variant nucleoside is associated with the number of CAG repeats

Pleiotropic Changes in Cycloheximideresistant Insect Cell Clones

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