Ahmad M. Alahmad
Kuwait City, KU, Kuwait
Last Updated: 09/26/2026
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Found 17 publications
TTC19-related mitochondrial complex III deficiency: Clinical and genetic characterization of 10 patients from 5 unrelated Arab families.
Journal: Molecular genetics and metabolism
Published: October 07, 2025
TTC19-related mitochondrial complex III deficiency: Clinical and genetic characterization of 10 patients from 5 unrelated Arab families.
Journal: Molecular genetics and metabolism
Published: October 07, 2025
A Homozygous Founder ELAC2 Variant in Kuwaiti Infants With Fatal Cardiomyopathy and Refractory Severe Lactic Acidosis: A Retrospective Review of the Clinical, Cardiological and Molecular Findings.
Journal: Molecular genetics & genomic medicine
Published: September 18, 2025
Insights from the Newborn Screening Program for Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency in Kuwait.
Journal: International journal of neonatal screening
Published: January 24, 2025
Static Loading of Different Intraradicular Preparation Depths of Trinia Endocrowns in Maxillary Canines.
Journal: The journal of contemporary dental practice
Published: October 04, 2024
Biallelic NDUFA13 variants lead to a neurodevelopmental phenotype with gradual neurological impairment.
Journal: Brain communications
Published: July 02, 2024
Removal Efficiency and Effectiveness of Four Different Fiber Posts Using Five Different Drill Systems in Multirooted Teeth.
Journal: The journal of contemporary dental practice
Published: March 21, 2024
Tribal Founder EMC1 Variant in 5 Kuwaiti Families Expands Phenotypic Spectrum of EMC1-Related Disorder.
Journal: Neurology. Genetics
Published: January 16, 2024
Biotin-thiamine responsive basal ganglia disease: a retrospective review of the clinical, radiological and molecular findings of cases in Kuwait with novel variants.
Journal: Orphanet journal of rare diseases
Published: February 20, 2023
A review of advanced technologies available to improve the healthcare performance during COVID-19 pandemic.
Journal: Procedia computer science
Published: January 23, 2023
LYRM7-associated mitochondrial complex III deficiency with non-cavitating leukoencephalopathy and stroke-like episodes.
Journal: American journal of medical genetics. Part A
Published: November 18, 2022
Bi-allelic LETM1 variants perturb mitochondrial ion homeostasis leading to a clinical spectrum with predominant nervous system involvement.
Journal: American journal of human genetics
Published: March 27, 2022
Last Updated: 09/26/2026