Results 231 to 240 of about 7,570,159 (401)
LINC00323 variant is associated with increased risk of essential tremor
Annals of Clinical and Translational Neurology, EarlyView.Abstract Essential tremor (ET) is a common adult movement disorder, with accumulating evidence suggesting that genetic factors primarily account for ET risk. However, replication studies on the genetic variants have yielded inconsistent results. In our case–control study, we show that the LINC00323 variant, identified in a European GWAS study, is ...
Brendan Tan +11 more
wiley +1 more source
A Lecture ON SOME OF THE LESS COMMON ASPECTS OF PNEUMONIA: Delivered to the York Medical Society [PDF]
, 1910 Tony Oliver
openalex +1 more source
UDP‐glucose dehydrogenase variants cause dystroglycanopathy
Annals of Clinical and Translational Neurology, EarlyView.Abstract UDP‐glucose dehydrogenase (UGDH) variants have been associated with hypotonia, developmental delay, and epilepsy. We report the first pathologic evidence of dystroglycanopathy in siblings with UGDH variants. Both presented around 6 months with developmental delay and elevated creatinine kinase.
Anna M. Reelfs +8 more
wiley +1 more source
Doctors, Medical Societies and the Pharmaceutical Industry
Canadian Respiratory Journal, 2002 Irvin Mayers
doaj +1 more source
JACMP – Founding and 2000–2004
Journal of Applied Clinical Medical Physics, EarlyView.
Michael Mills
wiley +1 more source
Early BMI Change, Cognitive Decline, and CSF AD Biomarkers Alterations in Parkinson's Disease
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective To examine the relationship of early BMI change with subsequent cognitive decline, CSF AD biomarkers alterations, and progression to dementia in patients with PD. Methods Study data were prospectively collected from the PPMI cohort. Weight/height data at enrollment and second‐year clinical visit were utilized to calculate BMI change.
Rui Zhong, Kezhong Zhang
wiley +1 more source
An Address on Acute Manifestations of Chronic Disease: Delivered at the Opening of the Winter Session of the Midland Medical Society [PDF]
, 1902 J Mitchell Bruce
openalex +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who
Sara Rubio‐Guerra +17 more
wiley +1 more source
COVID-19 and ethical considerations: Valuable decision-making tools from the leading medical societies in France. [PDF]
Anaesth Crit Care Pain Med, 2020 Lamblin A, de Montgolfier S.
europepmc +1 more source