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Sib-pair subgroup familial type 1 diabetes mellitus in children in the state of Qatar

PloS one, 2022-07, Vol.17 (7), p.e0271182-e0271182

2022

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Somatostatin analogues for the treatment of hyperinsulinaemic hypoglycaemia

Therapeutic Advances in Endocrinology and Metabolism, 2020, Vol.11, p.2042018820965068-2042018820965068

2020

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Clinical features, epidemiology, autoantibody status, HLA haplotypes and genetic mechanisms of type 1 diabetes mellitus among children in Qatar

Scientific reports, 2021-09, Vol.11 (1), p.18887-18887, Article 18887

2021

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Case Report: Hepatic Adenomatosis in a Patient With Prader-Willi Syndrome

Frontiers in endocrinology (Lausanne), 2022-03, Vol.13, p.826772

2022

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The epidemiology, clinical, biochemical, immunological and radiological features of youth onset type 2 diabetes mellitus in the state of Qatar

Diabetology international, 2022-04, Vol.13 (2), p.381-386

2022

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Case Report: Phenotype-Gene Correlation in a Case of Novel Tandem 4q Microduplication With Short Stature, Speech Delay and Microcephaly

Frontiers in endocrinology (Lausanne), 2022-02, Vol.12, p.783235

2022

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Severe Growth Hormone Deficiency in an Indian Boy Caused by a Novel 6 kb Homozygous Deletion Spanning the GH1 Gene

Journal of clinical research in pediatric endocrinology, 2024-06, Vol.16 (2), p.229-234

2024

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Epidemiology, genetic landscape and classification of childhood diabetes mellitus in the State of Qatar

Journal of diabetes investigation, 2021-12, Vol.12 (12), p.2141-2148

2021

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Maturity‐onset diabetes of the young (MODY) due to PDX1 mutation in a sib‐pair diabetes family from Qatar

Clinical case reports, 2021-12, Vol.9 (12), p.e05141-n/a

2021

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Infancy onset diabetes mellitus in a patient with a novel homozygous LRBA mutation

Journal of clinical and translational endocrinology case reports, 2022-03, Vol.23, p.100108, Article 100108

2022

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Understanding the Mechanism of Dysglycemia in a Fanconi-Bickel Syndrome Patient

Frontiers in endocrinology (Lausanne), 2022-05, Vol.13, p.841788-841788

2022

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Single-Center Experience of Using Liraglutide in Adolescents With Obesity +/- Type 2 Diabetes

Curēus (Palo Alto, CA), 2024-04

2024

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Understanding the Role of GLUT2 in Dysglycemia Associated with Fanconi-Bickel Syndrome

Biomedicines, 2022-08, Vol.10 (9), p.2114

2022

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The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the state of Qatar

Molecular genetics & genomic medicine, 2019-10, Vol.7 (10), p.e00753-n/a

2019

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A SLC16A1 Mutation in an Infant With Ketoacidosis and Neuroimaging Assessment: Expanding the Clinical Spectrum of MCT1 Deficiency

Frontiers in pediatrics, 2019-07, Vol.7, p.299

2019

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A Novel Homozygous MC2R Variant Leading to Type-1 Familial Glucocorticoid Deficiency

Journal of the Endocrine Society, 2022-06, Vol.6 (6), p.bvac058-bvac058

2022

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Managing Severe Hypoglycaemia in Patients with Diabetes: Current Challenges and Emerging Therapies

Diabetes, metabolic syndrome and obesity, 2023-01, Vol.16, p.259-273

2023

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Rare Antagonistic Leptin Variants and Severe, Early-Onset Obesity

The New England journal of medicine, 2023-06, Vol.388 (24), p.2253-2261

2023

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Understanding the Genetics of Early-Onset Obesity in a Cohort of Children From Qatar

The journal of clinical endocrinology and metabolism, 2023-11, Vol.108 (12), p.3201-3213

2023

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Type 2 Diabetes Mellitus in a 7 Year Old Girl

International medical case reports journal, 2022-05, Vol.15, p.245-250

2022

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Prediabetes in Children: A Single Center Experience from Qatar

SVOA Paediatrics, 2024-06, Vol.3 (4), p.72-78

2024

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The prevalence, immune profile, and clinical characteristics of children with celiac disease and type 1 diabetes mellitus in the state of Qatar

Journal of Pediatric Endocrinology and Metabolism, 2021-11, Vol.34 (11), p.1457-1461

2021

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Homozygous Insulin Promotor Gene Mutation Causing Permanent Neonatal Diabetes Mellitus and Childhood Onset Autoantibody Negative Diabetes in the Same Family

International medical case reports journal, 2022-01, Vol.15, p.35-41

2022

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The Epidemiology and Genetic Analysis of Children With Idiopathic Type 1 Diabetes in the State of Qatar

Journal of the Endocrine Society, 2021-10, Vol.5 (10), p.bvab131-bvab131

2021

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Type 2 Diabetes Mellitus in a 7 Year Old Girl

International medical case reports journal, 2022, Vol.15, p.245-250

2022

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Sib-pair subgroup familial type 1 diabetes mellitus in children in the state of Qatar

Somatostatin analogues for the treatment of hyperinsulinaemic hypoglycaemia

Clinical features, epidemiology, autoantibody status, HLA haplotypes and genetic mechanisms of type 1 diabetes mellitus among children in Qatar

Case Report: Hepatic Adenomatosis in a Patient With Prader-Willi Syndrome

The epidemiology, clinical, biochemical, immunological and radiological features of youth onset type 2 diabetes mellitus in the state of Qatar

Case Report: Phenotype-Gene Correlation in a Case of Novel Tandem 4q Microduplication With Short Stature, Speech Delay and Microcephaly

Severe Growth Hormone Deficiency in an Indian Boy Caused by a Novel 6 kb Homozygous Deletion Spanning the GH1 Gene

Epidemiology, genetic landscape and classification of childhood diabetes mellitus in the State of Qatar

Maturity‐onset diabetes of the young (MODY) due to PDX1 mutation in a sib‐pair diabetes family from Qatar

Infancy onset diabetes mellitus in a patient with a novel homozygous LRBA mutation

Understanding the Mechanism of Dysglycemia in a Fanconi-Bickel Syndrome Patient

Single-Center Experience of Using Liraglutide in Adolescents With Obesity +/- Type 2 Diabetes

Understanding the Role of GLUT2 in Dysglycemia Associated with Fanconi-Bickel Syndrome

The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the state of Qatar

A SLC16A1 Mutation in an Infant With Ketoacidosis and Neuroimaging Assessment: Expanding the Clinical Spectrum of MCT1 Deficiency

A Novel Homozygous MC2R Variant Leading to Type-1 Familial Glucocorticoid Deficiency

Managing Severe Hypoglycaemia in Patients with Diabetes: Current Challenges and Emerging Therapies

Rare Antagonistic Leptin Variants and Severe, Early-Onset Obesity

Understanding the Genetics of Early-Onset Obesity in a Cohort of Children From Qatar

Type 2 Diabetes Mellitus in a 7 Year Old Girl

Prediabetes in Children: A Single Center Experience from Qatar

The prevalence, immune profile, and clinical characteristics of children with celiac disease and type 1 diabetes mellitus in the state of Qatar

Homozygous Insulin Promotor Gene Mutation Causing Permanent Neonatal Diabetes Mellitus and Childhood Onset Autoantibody Negative Diabetes in the Same Family

The Epidemiology and Genetic Analysis of Children With Idiopathic Type 1 Diabetes in the State of Qatar

Type 2 Diabetes Mellitus in a 7 Year Old Girl

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