Nadjar Y - Search Results

1

Association between divalent metal transport 1 encoding gene (SLC11A2) and disease duration in amyotrophic lateral sclerosis.

Blasco H, Vourc'h P, Nadjar Y, Ribourtout B, Gordon PH, Guettard YO, Camu W, Praline J, Meininger V, Andres CR, Corcia P; French ALS study group. Blasco H, et al. Among authors: nadjar y. J Neurol Sci. 2011 Apr 15;303(1-2):124-7. doi: 10.1016/j.jns.2010.12.018. Epub 2011 Jan 26. J Neurol Sci. 2011. PMID: 21276595

2

Elevated serum ferritin is associated with reduced survival in amyotrophic lateral sclerosis.

Nadjar Y, Gordon P, Corcia P, Bensimon G, Pieroni L, Meininger V, Salachas F. Nadjar Y, et al. PLoS One. 2012;7(9):e45034. doi: 10.1371/journal.pone.0045034. Epub 2012 Sep 14. PLoS One. 2012. PMID: 23024788 Free PMC article.

3

Cerebral folate deficiency in adults: A heterogeneous potentially treatable condition.

Masingue M, Benoist JF, Roze E, Moussa F, Sedel F, Lubetzki C, Nadjar Y. Masingue M, et al. Among authors: nadjar y. J Neurol Sci. 2019 Jan 15;396:112-118. doi: 10.1016/j.jns.2018.11.014. Epub 2018 Nov 10. J Neurol Sci. 2019. PMID: 30448717

4

Brain White Matter Lesions and Presumed Crohn's Disease: Did You Consider MNGIE?

Cousyn L, Boehm V, Shor N, Treton X, Benamouzig R, Gaignard P, Nadjar Y. Cousyn L, et al. Among authors: nadjar y. Can J Neurol Sci. 2020 Jul;47(4):572-575. doi: 10.1017/cjn.2020.41. Epub 2020 Mar 3. Can J Neurol Sci. 2020. PMID: 32122424 No abstract available.

5

A juvenile ALS-like phenotype dramatically improved after high-dose riboflavin treatment.

Carreau C, Lenglet T, Mosnier I, Lahlou G, Fargeot G, Weiss N, Demeret S, Salachas F, Veauville-Merllié A, Acquaviva C, Nadjar Y. Carreau C, et al. Among authors: nadjar y. Ann Clin Transl Neurol. 2020 Feb;7(2):250-253. doi: 10.1002/acn3.50977. Epub 2020 Feb 5. Ann Clin Transl Neurol. 2020. PMID: 32022482 Free PMC article.

6

Natural history of cerebrotendinous xanthomatosis: a paediatric disease diagnosed in adulthood.

Degos B, Nadjar Y, Amador Mdel M, Lamari F, Sedel F, Roze E, Couvert P, Mochel F. Degos B, et al. Among authors: nadjar y. Orphanet J Rare Dis. 2016 Apr 16;11:41. doi: 10.1186/s13023-016-0419-x. Orphanet J Rare Dis. 2016. PMID: 27084087 Free PMC article.

7

Evolution of structural neuroimaging biomarkers in a series of adult patients with Niemann-Pick type C under treatment.

Masingue M, Adanyeguh I, Nadjar Y, Sedel F, Galanaud D, Mochel F. Masingue M, et al. Among authors: nadjar y. Orphanet J Rare Dis. 2017 Feb 2;12(1):22. doi: 10.1186/s13023-017-0579-3. Orphanet J Rare Dis. 2017. PMID: 28148276 Free PMC article.

8

Adolescence/adult onset MTHFR deficiency may manifest as isolated and treatable distinct neuro-psychiatric syndromes.

Gales A, Masingue M, Millecamps S, Giraudier S, Grosliere L, Adam C, Salim C, Navarro V, Nadjar Y. Gales A, et al. Among authors: nadjar y. Orphanet J Rare Dis. 2018 Feb 1;13(1):29. doi: 10.1186/s13023-018-0767-9. Orphanet J Rare Dis. 2018. PMID: 29391032 Free PMC article. Review.

9

Adolescent-Onset and Adult-Onset Vitamin-Responsive Neurogenetic Diseases: A Review.

Mandia D, Shor N, Benoist JF, Nadjar Y. Mandia D, et al. Among authors: nadjar y. JAMA Neurol. 2021 Apr 1;78(4):483-490. doi: 10.1001/jamaneurol.2020.4911. JAMA Neurol. 2021. PMID: 33427863 Review.

10

Diagnostic approach in adult-onset neurometabolic diseases.

Fernández-Eulate G, Carreau C, Benoist JF, Lamari F, Rucheton B, Shor N, Nadjar Y. Fernández-Eulate G, et al. Among authors: nadjar y. J Neurol Neurosurg Psychiatry. 2022 Apr;93(4):413-421. doi: 10.1136/jnnp-2021-328045. Epub 2022 Feb 9. J Neurol Neurosurg Psychiatry. 2022. PMID: 35140137 Free PMC article. Review.

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