Results 151 to 160 of about 5,067,029 (185)

Viral and non-viral cellular therapies for neurodegeneration. [PDF]

Front Med (Lausanne)
Srivastav J, Sharma S.
europepmc   +1 more source

Living with Risk, Aging with Uncertainty: A Narrative Review of Health and Genetic Vulnerability in Huntington's Disease. [PDF]

Biomedicines
Muñoz-Ortega AV, Conde Caballero D, Mariano Juárez L.   +2 more
europepmc   +1 more source

Interleaved stimulation in globus pallidus internus deep brain stimulation in a case of adult-onset Huntington's disease. [PDF]

BMC Neurol
Liu K, Wan S, Wang H, Zhao J, Chen X, Shu H, Yu S.   +6 more
europepmc   +1 more source

Reading Between the Striatal Lines: Magnetic Resonance Imaging Insights Into Huntington Disease. [PDF]

Ochsner J
Boothe R, Houghton DJ, Milburn J.
europepmc   +1 more source

Current knowledge of Huntington's disease-like 2 genetic testing, clinical presentation, and patient experiences: A systematic review. [PDF]

J Huntingtons Dis
Hoffmann K, White S, Sexton A.
europepmc   +1 more source

<i>Sesamum indicum</i>-derived valdiate as a novel neuroprotective agent targeting PDE10A2 and SIRT1 in Huntington's disease. [PDF]

Front Bioinform
Shyam M, Ismail MDW, Sharma D, Srirangan P, Muniyan R, Prince SE.   +5 more
europepmc   +1 more source

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Juvenile Huntington disease

Journal of Paediatrics and Child Health, 2006
Abstract:  Huntington disease (HD) is a dominantly inherited neurodegenerative disorder related to expansion of a triplet repeat sequence in the huntington gene on chromosome 4. Adult HD usually presents with chorea and personality changes. Juvenile HD is far less common and presents with parkinsonism, dystonia and seizures.
Nimeshan, Geevasinga, Fiona H, Richards, Kristi J, Jones, Monique M, Ryan   +3 more
openaire   +2 more sources

Juvenile Huntington disease

Human Genetics, 1986
Of 195 cases of juvenile Huntington disease gathered from case descriptions, the sex, age at onset, duration of disease, clinical type, sex of the affected parent, as well as sex, mean age at onset and at death of adult cases in the same pedigrees were noted when available, and the data were investigated for evidence of relationships between different ...
J G, van Dijk, E A, van der Velde, R A, Roos, G W, Bruyn   +3 more
openaire   +2 more sources

Anaesthesia and juvenile Huntington's disease

Pediatric Anesthesia, 2000
SummaryJuvenile Huntington's Disease (JHD) is an involuntary movement disorder that comprises both neurological and psychiatric symptoms. Whilst it has many similarities to Huntington's Disease, it is regarded as a separate clinical entity. The anaesthetic plan should be based on careful assessment of the important issues, including the risk of ...
K, Gupta, C P, Leng
openaire   +2 more sources

Juvenile Huntington disease in the Netherlands

Pediatric Neurology, 1997
Juvenile Huntington disease (JHD) patients are distinguished from adult patients by an age at onset of less than 20 years. Investigating patients in our own database, we examined the proposition derived from studies in world literature that JHD should not be viewed as a separate clinical entity but rather as a manifestation of the rigid variant of the ...
S, Siesling, M, Vegter-van der Vlis, R A, Roos   +2 more
openaire   +2 more sources