Ahmad Alahmad - Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Newcastle University

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论文共 11 篇作者统计合作学者相似作者

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Tribal Founder EMC1 Variant in 5 Kuwaiti Families Expands Phenotypic Spectrum of EMC1 -Related Disorder

Nada T. Alzayed, Abdullah H. Alzuabi, Reem A. Alqusaimi, Ehab A. El-Anany, Abdullah Alholle,Ashraf H. Aboelanine, Sherief Omar,Rasha Alsafi,Alaa A. Elmonairy, Fatemah J. Alali,Ahmad Alahmad,Hind Alsharhan,Buthaina Albash,Dana Marafi

NEUROLOGY-GENETICSno. 3 (2024)

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LYRM7‐associated Mitochondrial Complex III Deficiency with Non‐cavitating Leukoencephalopathy and Stroke‐like Episodes

Rita Alfattal, Maryam Alfarhan,Adeeb M. Algaith,Buthaina Albash,Reem M. Elshafie,Asma Alshammari,Ahmad Alahmad,Fatima Dashti,Rasha Alsafi,Hind Alsharhan

AMERICAN JOURNAL OF MEDICAL GENETICS PART A（2023）

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Biotin-thiamine Responsive Basal Ganglia Disease: a Retrospective Review of the Clinical, Radiological and Molecular Findings of Cases in Kuwait with Novel Variants

Maryam Aburezq,Ahmad Alahmad,Rasha Alsafi,Asma Al-Tawari,Dina Ramadan, Magdy Shafik,Omar Abdelaty,Nawal Makhseed, Reem Elshafie,Mariam Ayed, Abrar Hayat,Fatima Dashti,Dana Marafi,Buthaina Albash,Laila Bastaki,Hind Alsharhan

ORPHANET JOURNAL OF RARE DISEASESno. 1 (2023)

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Bi-allelic LETM1 Variants Perturb Mitochondrial Ion Homeostasis Leading to a Clinical Spectrum with Predominant Nervous System Involvement

Rauan Kaiyrzhanov,Sami E. M. Mohammed,Reza Maroofian,Ralf A. Husain,Alessia Catania,Alessandra Torraco,Ahmad Alahmad,Marina Dutra-Clarke,Sabine Gronborg,Annapurna Sudarsanam,Julie Vogt,Filippo Arrigoni,Julia Baptista,Shahzad Haider,Rene G. Feichtinger,Paolo Bernardi,Alessandra Zulian,Mirjana Gusic,Stephanie Efthymiou,Renkui Bai,Farah Bibi,Alejandro Horga, Julian A. Martinez-Agosto,Amanda Lam,Andreea Manole,Diego-Perez Rodriguez,Romina Durigon,Angela Pyle,Buthaina Albash,Carlo Dionisi-Vici, David Murphy,Diego Martinelli,Enrico Bugiardini,Katrina Allis,Costanza Lamperti,Siegfried Reipert, Lotte Risom,Lucia Laugwitz,Michela Di Nottia,Robert McFarland, Laura Vilarinho,Michael Hanna,Holger Prokisch,Johannes A. Mayr,Enrico Silvio Bertini,Daniele Ghezzi,Elsebet Ostergaard,Saskia B. Wortmann,Rosalba Carrozzo,Tobias B. Haack, Robert W. Taylor,Antonella Spinazzola,Karin Nowikovsky,Henry Houlden

American journal of human genetics（2022）

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Identification and Characterization of Novel MPC1 Gene Variants Causing Mitochondrial Pyruvate Carrier Deficiency

Huafang Jiang,Ahmad Alahmad,Song Fu,Xiaoling Fu,Zhimei Liu,Xiaodi Han,Lanlan Li,Tianyu Song,Manting Xu,Shanshan Liu,Junling Wang,Buthaina Albash, Ahmad Alaqeel,Vasilescu Catalina,Holger Prokisch,Robert W. Taylor,Robert McFarland, Fang

Journal of inherited metabolic disease（2022）

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Ep001: Newborn Screening Experience for Very Long Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency in Kuwait

Fatima Alabdulrazzaq,Hind AlSharhan,Amir Ahmed,Makia Marafie, Ibrahim Sulaiman, Reem Alshafie,Ahmad AlAhmad,Buthaina AlBash,Naser Ali, Parakkal Cyril, Usama Alkazzaz, Samia Ibrahim, Yasser Elfeky,Ayman Salloum,Asma Alshammari,Rehab Abdelrahman,Rasha Alsafi,Dina Ramadan,May Al-Rushood,Laila Bastaki

GENETICS IN MEDICINE（2022）

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Early Diagnosis of Classic Homocystinuria in Kuwait Through Newborn Screening: A 6-Year Experience

Hind Alsharhan, Amir A. Ahmed,Naser M. Ali,Ahmad Alahmad,Buthaina Albash,Reem M. Elshafie, Sumaya Alkanderi, Usama M. Elkazzaz, Parakkal Xavier Cyril,Rehab M. Abdelrahman,Alaa A. Elmonairy, Samia M. Ibrahim, Yasser M. E. Elfeky, Doaa Sadik, Sara D. Al-Enezi,Ayman M. Salloum,Yadav Girish, Mohammad Al-Ali,Dina G. Ramadan,Rasha Alsafi,May Al-Rushood,Laila Bastaki

International journal of neonatal screening（2021）

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Mitochondrial Disorders in the Arab Middle East Population: the Impact of Next Generation Sequencing on the Genetic Diagnosis

Ahmad Alahmad, Hebatallah Muhammad,Angela Pyle,Buthaina Albash,Robert McFarland,Robert Taylor

Journal of Biochemical and Clinical Geneticspp.54-64, (2019)

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