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Zerem, Ayelet
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1

Inventory of current practices regarding hematopoietic stem..:

Schoenmakers, Daphne H. ; Mochel, Fanny ; Adang, Laura A....
Orphanet Journal of Rare Diseases.  19 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
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2

Consensus guidelines for the monitoring and management of m..:

Adang, Laura A. ; Bonkowsky, Joshua L. ; Boelens, Jaap Jan...
Cytotherapy.  26 (2024)  7 - p. 739-748 , 2024
Link: https://doi.org/10.1016/..
 
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3

Newborn screening in metachromatic leukodystrophy – Europea..:

Laugwitz, Lucia ; Schoenmakers, Daphne H. ; Adang, Laura A....
European Journal of Paediatric Neurology.  49 (2024)  - p. 141-154 , 2024
Link: https://doi.org/10.1016/..
 
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4

Consequences of vestibular hypofunction in children with AD..:

Gur-Hartman, Tamar ; Tarrasch, Ricardo ; Zerem, Ayelet...
European Journal of Paediatric Neurology.  52 (2024)  - p. 1-9 , 2024
Link: https://doi.org/10.1016/..
 
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5

Utility of genetic testing in children with leukodystrophy:

Zerem, Ayelet ; Libzon, Stephanie ; Ben Sira, Liat...
European Journal of Paediatric Neurology.  45 (2023)  - p. 29-35 , 2023
Link: https://doi.org/10.1016/..
 
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6

Modified Delphi procedure-based expert consensus on endpoin..:

Schoenmakers, Daphne H. ; Beerepoot, Shanice ; van den Berg, Sibren...
Orphanet Journal of Rare Diseases.  17 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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7

White matter abnormalities and iron deposition in prenatal ..:

Zerem, Ayelet ; Ben-Sira, Liat ; Vigdorovich, Nitzan...
Metabolic Brain Disease.  36 (2021)  7 - p. 2155-2167 , 2021
Link: https://doi.org/10.1007/..
 
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8

Clinical phenotypes of infantile onset CACNA1A-related diso..:

Gur-Hartman, Tamar ; Berkowitz, Oren ; Yosovich, Keren...
European Journal of Paediatric Neurology.  30 (2021)  - p. 144-154 , 2021
Link: https://doi.org/10.1016/..
 
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9

Further Delineation of the Clinical and Pathologic Features..:

Helman, Guy ; Zerem, Ayelet ; Almad, Akshata...
Pediatric Neurology.  121 (2021)  - p. 11-19 , 2021
Link: https://doi.org/10.1016/..
 
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10

Expanding the genotype-phenotype spectrum of ISCA2-related ..:

Hartman, Tamar Gur ; Yosovich, Keren ; Michaeli, Hila Gur...
neurogenetics.  21 (2020)  4 - p. 243-249 , 2020
Link: https://doi.org/10.1007/..
 
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11

Autosomal dominant TUBB3-related syndrome: Fetal, radiologi..:

Blumkin, Lubov ; Leibovitz, Zvi ; Krajden-Haratz, Karina...
European Journal of Paediatric Neurology.  26 (2020)  - p. 46-60 , 2020
Link: https://doi.org/10.1016/..
 
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12

Metabolic stroke in a patient with bi-allelic OPA1 mutation:

Zerem, Ayelet ; Yosovich, Keren ; Rappaport, Yael Cohen...
Metabolic Brain Disease.  34 (2019)  4 - p. 1043-1048 , 2019
Link: https://doi.org/10.1007/..
 
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13

Brain white matter abnormalities associated with copy numbe..:

Vigdorovich, Nitzan ; Ben‐Sira, Liat ; Blumkin, Lubov...
American Journal of Medical Genetics Part A.  182 (2019)  1 - p. 93-103 , 2019
Link: https://doi.org/10.1002/..
 
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14

De novo hotspot variants in CYFIP2 cause early‐onset epilep..:

Nakashima, Mitsuko ; Kato, Mitsuhiro ; Aoto, Kazushi...
Annals of Neurology.  83 (2018)  4 - p. 794-806 , 2018
Link: https://doi.org/10.1002/..
 
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15

Expanding the phenotype of IBA57 mutations: related leukody..:

Hamanaka, Kohei ; Miyatake, Satoko ; Zerem, Ayelet...
Journal of Human Genetics.  63 (2018)  12 - p. 1223-1229 , 2018
Link: https://doi.org/10.1038/..
 
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