Results 121 to 130 of about 2,684 (177)

Differences in the Impact of Intensive Rehabilitation on Hereditary Ataxias and the Cerebellar Subtype of Multiple System Atrophy. [PDF]

Cerebellum
Bando K, Kondo Y, Miyazaki Y, Hara T, Takahashi Y.   +4 more
europepmc   +1 more source

Marriage Patterns and Pediatric Neurologicdisease in Damascus, Syria [PDF]

, 2007
Al-Rifai, Muhammad Talal, Woody, Robert C.   +1 more
core   +1 more source

Novel In-Frame FGF14 Deletion Causes Spinocerebellar Ataxia Type 27A: Clinical Response to Deep Brain Stimulation and 4-Aminopyridine. [PDF]

Mov Disord
Keller Sarmiento IJ, Bovenzi R, Kinsinger M, Kinsley L, Bustos BI, Krainc D, Mencacci NE.   +6 more
europepmc   +1 more source

A Novel Exon Duplication in the <i>SACS</i> Gene in Charlevoix-Saguenay Ataxia and a Summary of Polish Cases. [PDF]

Appl Clin Genet
Fichna JP, Elert-Dobkowska E, Radziwonik-Fraczyk W, Ziora-Jakutowicz K, Wężyk MM, Berdyński M, Zaremba J, Żekanowski C, Bednarska-Makaruk M.   +8 more
europepmc   +1 more source

A Scoping Review of POLG-Related Cerebellar Ataxia: Insights and Clinical Perspectives. [PDF]

Tremor Other Hyperkinet Mov (N Y)
Kalampokini S, Keramidiotis I, Ravanidis S, Lochner P, Kimiskidis VK, Hadjigeorgiou GM.   +5 more
europepmc   +1 more source

The efficacy of repetitive transcranial magnetic stimulation in patients with spinocerebellar ataxia: A systematic review and meta-analysis. [PDF]

J Chin Med Assoc
Lin YC, Kuo SH, Lin CP, Chang LH.
europepmc   +1 more source

Ataxia in Africa: current efforts and recommendations. [PDF]

Ann Med Surg (Lond)
Nebieridze A, Uwishema O, Jaafer Al Tarawneh Y, I Abdelsamea A, Zrara N, Albright Belise M, Mshaymesh S.   +6 more
europepmc   +1 more source

Digital Outcomes of Upper Limb Ataxia Capture Meaningful Longitudinal Change and Treatment Response. [PDF]

Mov Disord
Hermle D, Schubert R, Barallon P, Ilg W, Schüle R, Reilmann R, Synofzik M, Traschütz A.   +7 more
europepmc   +1 more source

Diagnostic Spectrum in an "Atypical" Atypical Parkinsonism Syndrome Cohort: A Single Center Experience. [PDF]

J Mov Disord
Katragadda P, Holla VV, Kamble N, Mahale RR, Yadav R, Pal PK.   +5 more
europepmc   +1 more source

A Rare Homozygous AP4S1 Variant in Rwandan Siblings with Autosomal Recessive Hereditary Spastic Paraplegia Type 52 (SPG52). [PDF]

Genes (Basel)
Niyoyita S, Uwibambe E, Ndinkabandi J, Sesonga P, Niyongere JB, Tuyishimire B, Urugwiro A, Rwamatwara A, Isingizwe G, Mutamuliza J, Nsanzabaganwa C, Bukuru J, Rutagarama F, Mukaruziga A, Karangwa O, Ndatinya A, Nsanzabera M, Dukuze N, Mutesa L.   +18 more
europepmc   +1 more source