E-LIB Suche - Ergebnisse für: Charif, Majida

1

The human OPA1delTTAG mutation induces adult onset and prog..:

Affortit, Corentin ; Coyat, Carolanne ; Saidia, Anissa Rym...
Cellular and Molecular Life Sciences. 81 (2024) 1 - p. , 2024

Link: https://doi.org/10.1007/..

2

First report on chromosomal abnormalities in Eastern Morocc..:

Elidrissi Errahhali, Manal ; Elidrissi Errahhali, Mounia ; Ramdani, Sara...
Archives de Pédiatrie. 31 (2024) 2 - p. 112-116 , 2024

Link: https://doi.org/10.1016/..

3

Expanding the genetic spectrum of mitochondrial diseases in..:

Gouiza, Ismail ; Hechmi, Meriem ; Zioudi, Abir...
Frontiers in Genetics. 14 (2024) - p. , 2024

Link: https://doi.org/10.3389/..

4

A novel variant in BMPR1B causes acromesomelic dysplasia Gr..:

Lhousni, Saida ; Charif, Majida ; Derouich, Yassine...
Bone. 175 (2023) - p. 116860 , 2023

Link: https://doi.org/10.1016/..

5

Vitamin B1 deficiency leads to high oxidative stress and mt..:

Felhi, Rahma ; Sfaihi, Lamia ; Charif, Majida...
Metabolic Brain Disease. 38 (2023) 7 - p. 2489-2497 , 2023

Link: https://doi.org/10.1007/..

6

Population structure and genetic diversity of Moroccan cann..:

Benkirane, Chaymae ; Charif, Majida ; Müller, Christina M....
Genetic Resources and Crop Evolution. 71 (2023) 5 - p. 2037-2051 , 2023

Link: https://doi.org/10.1007/..

7

Autosomal recessive Leber hereditary optic neuropathy, a ne..:

Lenaers, Guy ; Beaulieu, Cléis ; Charif, Majida...
Brain. 146 (2023) 8 - p. 3156-3161 , 2023

Link: https://doi.org/10.1093/..

8

Clinical and genetic spectrums of 413 North African familie..:

Bouzidi, Aymane ; Charoute, Hicham ; Charif, Majida...
Orphanet Journal of Rare Diseases. 17 (2022) 1 - p. , 2022

Link: https://doi.org/10.1186/..

9

Molecular heterogeneity of β‐thalassemia variants in the Ea..:

Belmokhtar, Ihab ; Lhousni, Saida ; Elidrissi Errahhali, Mounia...
Molecular Genetics & Genomic Medicine. 10 (2022) 8 - p. , 2022

Link: https://doi.org/10.1002/..

10

Next-Generation Sequencing Identifies Novel PMPCA Variants ..:

Charif, Majida ; Chevrollier, Arnaud ; Gueguen, Naïg...
Genes. 13 (2022) 7 - p. 1202 , 2022

Link: https://doi.org/10.3390/..

11

A homozygous nonsense HECW2 variant is associated with neur..:

Krami, Al Mehdi ; Bouzidi, Aymane ; Charif, Majida...
European Journal of Medical Genetics. 65 (2022) 6 - p. 104515 , 2022

Link: https://doi.org/10.1016/..

12

First characterization of LTBP3 variants in two Moroccan fa..:

Nouara, Falah ; Amalou, Ghita ; Bouzidi, Aymane...
Archives of Oral Biology. 142 (2022) - p. 105518 , 2022

Link: https://doi.org/10.1016/..

13

The top 10 most frequently involved genes in hereditary opt..:

Rocatcher, Aude ; Desquiret-Dumas, Valérie ; Charif, Majida...
Brain. 146 (2022) 2 - p. 455-460 , 2022

Link: https://doi.org/10.1093/..

14

Next-generation sequencing of Tunisian Leigh syndrome patie..:

Hechmi, Meriem ; Charif, Majida ; Kraoua, Ichraf...
Bioscience Reports. 42 (2022) 9 - p. , 2022

Link: https://doi.org/10.1042/..

15

Cancer/Testis Antigen 55 is required for cancer cell prolif..:

Aurrière, Jade ; Goudenege, David ; Baechler, Simone A....
Mitochondrion. 64 (2022) - p. 19-26 , 2022

Link: https://doi.org/10.1016/..