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choline and Spastic Paraplegia, Hereditary

choline has been researched along with Spastic Paraplegia, Hereditary in 2 studies

Spastic Paraplegia, Hereditary: A group of inherited diseases that share similar phenotypes but are genetically diverse. Different genetic loci for autosomal recessive, autosomal dominant, and x-linked forms of hereditary spastic paraplegia have been identified. Clinically, patients present with slowly progressive distal limb weakness and lower extremity spasticity. Peripheral sensory neurons may be affected in the later stages of the disease. (J Neurol Neurosurg Psychiatry 1998 Jan;64(1):61-6; Curr Opin Neurol 1997 Aug;10(4):313-8)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Erichsen, AK1
Server, A1
Landrø, NI1
Sandvik, L1
Tallaksen, CM1
Pizzini, F1
Fatemi, AS1
Barker, PB1
Nagae-Poetscher, LM1
Horská, A1
Zimmerman, AW1
Moser, HW1
Bibat, G1
Naidu, S1

Other Studies

2 other studies available for choline and Spastic Paraplegia, Hereditary

ArticleYear
Proton magnetic resonance spectroscopy and cognition in patients with spastin mutations.
    Journal of the neurological sciences, 2009, Feb-15, Volume: 277, Issue:1-2

    Topics: Adenosine Triphosphatases; Adult; Aspartic Acid; Biomarkers; Choline; Cognition Disorders; Creatine;

2009
Proton MR spectroscopic imaging in Pelizaeus-Merzbacher disease.
    AJNR. American journal of neuroradiology, 2003, Volume: 24, Issue:8

    Topics: Aspartic Acid; Brain; Child; Child, Preschool; Choline; Creatine; Diagnosis, Differential; Dominance

2003