Wali GM[au] - Search Results

Year	Number of Results
1982	1
1985	1
1989	1
1991	1
1992	1
1993	1
1994	1
1999	2
2000	2
2001	1
2002	2
2003	1
2004	1
2005	1
2010	1
2011	1
2012	2
2013	1
2014	1
2016	1
2019	4
2020	2
2021	1
2023	0

1

Genetic analysis of a family from India with Machado-Joseph disease.

Anjanappa RM, Jain S, Wali GM, Purushottam M. Anjanappa RM, et al. Among authors: wali gm. Neurol India. 2019 Mar-Apr;67(2):582-588. doi: 10.4103/0028-3886.258030. Neurol India. 2019. PMID: 31085886 Free article. No abstract available.

2

Broadening the Clinical Spectrum of Very Low Density Lipoprotein Receptor Associated Dysequilibrium Syndrome.

Wali GM, Wali G. Wali GM, et al. Mov Disord Clin Pract. 2021 Apr 3;8(4):619-623. doi: 10.1002/mdc3.13184. eCollection 2021 May. Mov Disord Clin Pract. 2021. PMID: 33981800 Free PMC article. No abstract available.

3

Long-Term Follow-Up and Evolution of ADCY5-From a Ballistic to Dystonic Phenotype.

Wali GM, Wali G, Kumar KR, Sue CM. Wali GM, et al. Mov Disord Clin Pract. 2020 Sep 14;7(8):985-986. doi: 10.1002/mdc3.13069. eCollection 2020 Nov. Mov Disord Clin Pract. 2020. PMID: 34919601 Free PMC article. No abstract available.

4

A Novel Homozygous Mutation in the FUCA1 Gene Highlighting Fucosidosis as a Cause of Dystonia: Case Report and Literature Review.

Wali G, Wali GM, Sue CM, Kumar KR. Wali G, et al. Among authors: wali gm. Neuropediatrics. 2019 Aug;50(4):248-252. doi: 10.1055/s-0039-1684052. Epub 2019 May 7. Neuropediatrics. 2019. PMID: 31064022 Review.

5

Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypes.

Kumar KR, Davis RL, Tchan MC, Wali GM, Mahant N, Ng K, Kotschet K, Siow SF, Gu J, Walls Z, Kang C, Wali G, Levy S, Phua CS, Yiannikas C, Darveniza P, Chang FCF, Morales-Briceño H, Rowe DB, Drew A, Gayevskiy V, Cowley MJ, Minoche AE, Tisch S, Hayes M, Kummerfeld S, Fung VSC, Sue CM. Kumar KR, et al. Among authors: wali gm. Parkinsonism Relat Disord. 2019 Dec;69:111-118. doi: 10.1016/j.parkreldis.2019.11.004. Epub 2019 Nov 7. Parkinsonism Relat Disord. 2019. PMID: 31731261 Free article.

6

Parkinsonism associated with Addison's disease.

Wali GM. Wali GM. Mov Disord. 2003 Mar;18(3):340-342. doi: 10.1002/mds.10340. Mov Disord. 2003. PMID: 12621641

7

Molecular analysis of α-synuclein gene in Parkinson's disease in North Karnataka, India.

Kadakol GS, Kulkarni SS, Wali GM, Gai PB. Kadakol GS, et al. Among authors: wali gm. Neurol India. 2014 Mar-Apr;62(2):149-52. doi: 10.4103/0028-3886.132338. Neurol India. 2014. PMID: 24823723 Free article.

8

Myxoedema conditioned pellagra.

Desai SG, Wali GM. Desai SG, et al. Among authors: wali gm. J Indian Med Assoc. 1982 May;78(9-10):145-7. J Indian Med Assoc. 1982. PMID: 7130728 No abstract available.

9

Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing.

Kumar KR, Wali GM, Kamate M, Wali G, Minoche AE, Puttick C, Pinese M, Gayevskiy V, Dinger ME, Roscioli T, Sue CM, Cowley MJ. Kumar KR, et al. Among authors: wali gm. Neurogenetics. 2016 Oct;17(4):265-270. doi: 10.1007/s10048-016-0495-z. Epub 2016 Sep 28. Neurogenetics. 2016. PMID: 27679996 Free PMC article.

10

Sepiapterin reductase deficiency: a treatable mimic of cerebral palsy.

Friedman J, Roze E, Abdenur JE, Chang R, Gasperini S, Saletti V, Wali GM, Eiroa H, Neville B, Felice A, Parascandalo R, Zafeiriou DI, Arrabal-Fernandez L, Dill P, Eichler FS, Echenne B, Gutierrez-Solana LG, Hoffmann GF, Hyland K, Kusmierska K, Tijssen MA, Lutz T, Mazzuca M, Penzien J, Poll-The BT, Sykut-Cegielska J, Szymanska K, Thöny B, Blau N. Friedman J, et al. Among authors: wali gm. Ann Neurol. 2012 Apr;71(4):520-30. doi: 10.1002/ana.22685. Ann Neurol. 2012. PMID: 22522443

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