Results 231 to 240 of about 90,019 (314)

Expanding the clinical phenotype of DYNC1H1 -associated mutations: a Chinese family with autosomal dominant complex hereditary spastic paraplegia. [PDF]

BMC Med Genomics
Yuan X, Zhang S, Tang Y.
europepmc   +1 more source

The frozen elephant trunk technique. [PDF]

Nagoya J Med Sci
Mutsuga M.
europepmc   +1 more source

Neuroradiological Phenotype Expansion of the Siddiqi Syndrome: A Case Report. [PDF]

Cell Mol Neurobiol
Trilla P, Rodriguez-Revenga L, Sanchez A, Madrigal I, Milisenda JC, Muñoz E, Alvarez-Mora MI.   +6 more
europepmc   +1 more source

Rehabilitation with Intrathecal Baclofen and Gait Training Using Hybrid Assistive Limb in a Patient with Hereditary Spastic Paraplegia: A Case Report. [PDF]

Prog Rehabil Med
Asaeda M, Urabe M, Orita N, Maeda N, Ueda K, Araki T, Mikami Y.   +6 more
europepmc   +1 more source

Hereditary Spastic Paraplegia-Report of 2 Cases in a Family

, 2013
Kanij Fatema, Mizanur Rahman, Shaheen Akhter, Tahmina Karim   +3 more
openalex   +2 more sources

RAB3A variants in ataxia and other neurodegenerative disorders. [PDF]

Brain
Percetti M, Monfrini E, Del Bo R, Canesi M, Cavallieri F, Di Rauso G, Fioravanti V, Del Prete E, Frosini D, Palermo G, Ceravolo R, Sacilotto G, Di Fonzo A.   +12 more
europepmc   +1 more source

Editorial: Advances in spinal cord injury prevention during endovascular and open aortic repairs. [PDF]

Front Surg
Rahouma M, Baudo M, El-Sayed Ahmed M.
europepmc   +1 more source

Spinal Cord Infarction as an Atypical Thromboembolic Complication of First-Diagnosed Atrial Fibrillation. [PDF]

Int Med Case Rep J
Tyrikos G, Karakasis P, Nevras V, Zelevaris N, Nalmpantidou C, Gkounti G.   +5 more
europepmc   +1 more source

Life after the hospital: Lived experience of people with traumatic spinal cord injury in a resource-constrained setting - a qualitative study. [PDF]

S Afr J Physiother
Kanyoni M, Fitch MI, Phillips J, Nilsson-Wikmar L, Tumusiime DK.   +4 more
europepmc   +1 more source

Identification of myokymia in adult-onset hereditary spastic paraplegia type 79A: Implications for the phenotypic spectrum. [PDF]

eNeurologicalSci
Toyoda N, Komiya H, Miyaji Y, Nishihama S, Takeda M, Asano T, Hashiguchi S, Takahashi K, Higashiyama Y, Fujita A, Matsumoto N, Doi H, Tanaka F.   +12 more
europepmc   +1 more source