Publications by authors named "Moeenaldeen D AlSayed"

Claim this Profile
N
Natural history of SPTBN4-related neurodevelopmental disorder with hypotonia, neuropathy, and deafness.
Hanan AlQudairy, Mohammad A AlMuhaizea, Mohamed Tohary, Maissa Alfuraih, Aisha Alnafisah, Moeenaldeen D AlSayed

Orphanet J Rare Dis· August 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel UBE3B mutations: report of eight patients with Kaufman oculocerebrofacial syndrome with additional clinical findings from a highly consanguineous population.
AlBandary Albakheet, Duaa Almuallami, Rawan Almass, Alya Qari, Rosan Kenana, Moeenaldeen D AlSayed

Clin Dysmorphol· April 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
SLC25A42-associated mitochondrial encephalomyopathy: Report of additional founder cases and functional characterization of a novel deletion.
Mazhor Aldosary, Shahad Baselm, Maha Abdulrahim, Rawan Almass, Maysoon Alsagob, Moeenaldeen D AlSayed

JIMD Rep· July 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways.
Mazhor Aldosary, AlBandary Al-Bakheet, Hesham Al-Dhalaan, Rawan Almass, Maysoon Alsagob, Moeenaldeen D AlSayed

OMICS· March 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy.
Holger Hengel, Célia Bosso-Lefèvre, George Grady, Emmanuelle Szenker-Ravi, Hankun Li, Moeenaldeen D AlSayed

Nat Commun· January 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The effects of low protein products availability on growth parameters and metabolic control in selected amino acid metabolism disorders patients.
Bedour Handoom, Eman Megdad, Dana Al-Qasabi, Munirah Al Mesned, Reem Hawary, Moeenaldeen Dia Alsayed

Int J Pediatr Adolesc Med· June 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Impact of long-term elosulfase alfa on activities of daily living in patients with Morquio A syndrome in an open-label, multi-center, phase 3 extension study.
Christian J Hendriksz, Rossella Parini, Moeenaldeen D AlSayed, Julian Raiman, Roberto Giugliani

Mol Genet Metab· February 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Impact of long-term elosulfase alfa treatment on respiratory function in patients with Morquio A syndrome.
Christian J Hendriksz, Kenneth I Berger, Rossella Parini, Moeenaldeen D AlSayed, Julian Raiman

J Inherit Metab Dis· November 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Long-term endurance and safety of elosulfase alfa enzyme replacement therapy in patients with Morquio A syndrome.
Christian J Hendriksz, Rossella Parini, Moeenaldeen D AlSayed, Julian Raiman, Roberto Giugliani

Mol Genet Metab· September 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical, neuroimaging, and genetic features of L-2-hydroxyglutaric aciduria in Arab kindreds.
Muhammad Faiyaz-Ul-Haque, Moeenaldeen D Al-Sayed, Eissa Faqeih, Masood Jamil, Anjum Saeed

Ann Saudi Med· November 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mitochondrial Neurogastrointestinal Encephalomyopathy Treated with Stem Cell Transplantation: A Case Report and Review of Literature.
Musthafa Chalikandy Peedikayil, Eje Ingvar Kagevi, Ehab Abufarhaneh, Moeenaldeen Dia Alsayed, Hazzaa Abdulla Alzahrani

Hematol Oncol Stem Cell Ther· June 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Multi-domain impact of elosufase alfa in Morquio A syndrome in the pivotal phase III trial.
Christian J Hendriksz, Roberto Giugliani, Paul Harmatz, Eugen Mengel, Nathalie Guffon

Mol Genet Metab· February 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The development of genetic counseling services and training program in Saudi Arabia.
Alya A Qari, Ameera S Balobaid, Rifaat R Rawashdeh, Moeenaldeen D Al-Sayed

J Genet Couns· December 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delay.
Moeenaldeen D Al-Sayed, Hamad Al-Zaidan, Albandary Albakheet, Hana Hakami, Rosan Kenana

Am J Hum Genet· October 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis