Results 61 to 70 of about 1,908,985 (246)

Progressive Supranuclear Palsy in India: Insights from a Large Multicenter Clinical Cohort (Project PAIR‐PSP)

open access: yesMovement Disorders Clinical Practice, EarlyView.
Background Progressive supranuclear palsy (PSP) is a rare and devastating tauopathy with limited global data. Given India's large population, genetic diversity, and clinical heterogeneity, large multicenter datasets are crucial to enrich global understanding of PSP. Objective To characterize the demographic, clinical, and phenotypic profiles of a large
Prashanth Lingappa Kukkle   +31 more
wiley   +1 more source

JAK2 Variant and Parkinsonian Syndromes: Coincidence or Pathophysiological Link?

open access: yesMovement Disorders Clinical Practice, EarlyView.
Abstract Background JAK2 variants are a hallmark of myeloproliferative neoplasms (MPNs), including polycythemia vera and essential thrombocythemia. These disorders are often associated with thrombotic and inflammatory complications. From a movement disorder perspective, chorea is a rare but well‐recognized neurological occurrence in this context ...
Elena Ardila Jurado   +5 more
wiley   +1 more source

Effect of Acupuncture Intervention on Learning-memory Ability and Cerebral Superoxide Dis-mutase Activity and Malonaldehyde Concentration in Chronic Fatigue Syndrome Rats

open access: yes针刺研究, 2013
Objective To observe the effect of acupuncture intervention on learning-memory ability and cerebral superoxide dismutase(SOD)activity and malonaldehyde(MDA)content in chronic fatigure syndrome(CFS)rats so as to reveal its mechanism underlying improvement
LIU Chang-zheng, LEI Bo
doaj   +2 more sources

Principal component analysis of the effects of environmental enrichment and (-)-epigallocatechin-3-gallate on age-associated learning deficits in a mouse model of Down syndrome

open access: yesFrontiers in Behavioral Neuroscience, 2015
Down syndrome (DS) individuals present increased risk for Alzheimer disease (AD) neuropathology and AD-type dementia. Here, we investigated the use of green tea extracts containing (-)-epigallocatechin-3-gallate (EGCG), as co-adjuvant to enhance the ...
Silvina eCatuara-Solarz   +17 more
doaj   +1 more source

Letter: Thomas L. Morris to Ida M. Tarbell, November 1, 1899

open access: yes, 1899
Compared proof and original letter, A. Lincoln to I.N.
Morris, Thomas L.
core  

Lettre de Robert Christie à Alexander Morris sur l'absence de Morris lorsque Christie lui a rendu visite

open access: yes
2 pages, originalLettre de Robert Christie à Alexander Morris sur : l'absence de Morris lorsque Christie lui a rendu visite et un essai de Morris sur le ...
Christie, Robert;
core   +1 more source

Lettre de L. H. Holton à Alexander Morris sur l'entérinement, par le Gouvernement fédéral, de l'administration de Morris

open access: yes, 1875
4 pages, originalLettre de L. H. Holton à A[lexander] Morris sur : l'entérinement, par le Gouvernement fédéral, de l'administration de Morris; les efforts d'[Alexander] Mackenzie pour donner un poste ministériel à [Edward] Blake; l'échec d'un ...
Holton, Luther Hamilton;
core   +1 more source

Effect of repeated morphine withdrawal on spatial learning, memory and serum cortisol level in mice

open access: yesAdvanced Biomedical Research, 2013
Background: One of the serious problems that opioid addicted people are facing is repeated withdrawal syndrome that is accompanying with a significant stress load for addicts.
Mahdieh Matinfar   +6 more
doaj   +1 more source

Genetic Investigation in Fetal Growth Restriction: An Integrated Approach for Clinical Practice

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT International guidelines recommend genetic testing when fetal growth restriction (FGR) accompanies structural anomalies, but recommendations for apparently isolated FGR remain variable, particularly regarding gestational age thresholds and the role of exome sequencing (ES). Interpretation is difficult because studies define FGR inconsistently,
Eran Ashwal, David Chitayat
wiley   +1 more source

Complete androgen insensitivity syndrome in a 15-year-old female with primary amenorrhea and undescended testes: a rare case report

open access: yesRadiology Case Reports
Morris syndrome, also known as Complete Androgen Insensitivity Syndrome (CAIS), is a rare genetic disorder of sex development characterized by a 46, XY karyotype with female external genitalia due to androgen receptor mutations. We present a case of a 15-
Fariha Zerin, MBBS   +3 more
doaj   +1 more source

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