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AlSayed, Moeenaldeen
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1

Revealing the genetic complexity of long-chain fatty acid o..:

Baker II, Peter ; Miller, Vanessa Rangel ; Richbourg, Heather...
Molecular Genetics and Metabolism.  141 (2024)  4 - p. 108206 , 2024
Link: https://doi.org/10.1016/..
 
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2

European Achondroplasia Forum Practical Considerations for ..:

Fredwall, Svein ; AlSayed, Moeenaldeen ; Ben-Omran, Tawfeg...
Advances in Therapy.  41 (2024)  7 - p. 2545-2558 , 2024
Link: https://doi.org/10.1007/..
 
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3

P032: Decoding the genetic tapestry of long chain fatty aci..:

Miller, Vanessa Rangel ; Richbourg, Heather ; Vockley, Jerry...
Genetics in Medicine Open.  2 (2024)  - p. 100909 , 2024
Link: https://doi.org/10.1016/..
 
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4

European Achondroplasia Forum guiding principles for the de..:

Irving, Melita ; AlSayed, Moeenaldeen ; Arundel, Paul...
Orphanet Journal of Rare Diseases.  18 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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5

Real-world evidence in achondroplasia: considerations for a..:

Alanay, Yasemin ; Mohnike, Klaus ; Nilsson, Ola...
Orphanet Journal of Rare Diseases.  18 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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6

Expanding the allelic spectrum of ELOVL4‐related autosomal ..:

Alabdulrazzaq, Fatima ; Alanzi, Talal ; Al‐Balool, Haya H....
Molecular Genetics & Genomic Medicine.  11 (2023)  12 - p. , 2023
Link: https://doi.org/10.1002/..
 
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7

A Novel Homozygous Founder Variant of RTN4IP1 in Two Consan..:

Aldosary, Mazhor ; Alsagob, Maysoon ; AlQudairy, Hanan...
Cells.  11 (2022)  19 - p. 3154 , 2022
Link: https://doi.org/10.3390/..
 
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8

RETROSPECTIVE STUDY OF THE THE NATURAL HISTORY AND DISEASE ..:

AlSayed, Moeenaldeen ; Almasseri, Zainab
Molecular Genetics and Metabolism.  135 (2022)  4 - p. 258 , 2022
Link: https://doi.org/10.1016/..
 
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9

Optimising care and follow-up of adults with achondroplasia:

Fredwall, Svein ; Allum, Yana ; AlSayed, Moeenaldeen...
Orphanet Journal of Rare Diseases.  17 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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10

COVID-19 in Unvaccinated patients with inherited metabolic ..:

Altassan, Ruqaiah ; Sulaiman, Raashda A. ; Alfalah, Abdullah...
European Journal of Medical Genetics.  65 (2022)  11 - p. 104602 , 2022
Link: https://doi.org/10.1016/..
 
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11

RETROSPECTIVE STUDY OF THE THE NATURAL HISTORY AND DISEASE ..:

AlSayed, Moeenaldeen ; Almasseri, Zainab
Molecular Genetics and Metabolism.  135 (2022)  4 - p. 258-259 , 2022
Link: https://doi.org/10.1016/..
 
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12

Optimising the diagnosis and referral of achondroplasia in ..:

Cormier-Daire, Valerie ; AlSayed, Moeenaldeen ; Alves, Inês...
Orphanet Journal of Rare Diseases.  17 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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13

Gonadal mosaicism in GNAO1 causing neurodevelopmental disor..:

Al Masseri, Zainab ; AlSayed, Moeenaldeen
Molecular Genetics and Metabolism Reports.  31 (2022)  - p. 100864 , 2022
Link: https://doi.org/10.1016/..
 
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14

The first European consensus on principles of management fo..:

Cormier-Daire, Valerie ; AlSayed, Moeenaldeen ; Ben-Omran, Tawfeg...
Orphanet Journal of Rare Diseases.  16 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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15

Molecular basis of mucopolysaccharidosis IVA (Morquio A syn..:

Zanetti, Alessandra ; D'Avanzo, Francesca ; AlSayed, Moeenaldeen...
Human Mutation.  42 (2021)  11 - p. 1384-1398 , 2021
Link: https://doi.org/10.1002/..
 
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