Results 261 to 270 of about 1,156,853 (299)
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Clinical Variants of Pemphigoid

International Journal of Dermatology, 1986
H N, Liu, W P, Su, R S, Rogers
openaire   +4 more sources

Clinical variant of familial amyloid polyneuropathy

Muscle & Nerve, 2002
AbstractHereditary amyloidosis with early and prominent peripheral nerve involvement is often designated familial amyloid polyneuropathy (FAP). The abnormality usually lies in the transthyretin (TTR) gene. We describe a patient with a tyr77 TTR gene mutation who presented with sensorimotor polyneuropathy but no other systemic symptoms of amyloidosis ...
Dianna, Quan, Jeffrey A, Cohen
openaire   +2 more sources

Determination of the Clinical Significance of an Unclassified Variant

2011
After completion of Human Genome Project (HGP) in 2003, as well as the new technology development in genomic research, the most accurate genetics blueprint of human is available. Researchers started to dissect and understand the genetic map of the human species.
Victor Wei, Zhang, Jing, Wang
openaire   +2 more sources

Temporal Lobe Syncope: Clinical Variants

Clinical Electroencephalography, 1989
Temporal lobe syncope (TLS) is a term coined by Landolt. Characteristically, the patient has psychomotor and drop attacks, and the interictal electroencephalogram (EEG) shows temporal lobe epileptic abnormalities. TLS is synonymous with type III complex partial seizures (CPSs) in the Delgado Escueta classification.
openaire   +2 more sources

Clinical Delineation of Rett Syndrome Variants

Neuropediatrics, 1995
The broad clinical variety within the Rett syndrome (RS) concept is emphasized. A model recently presented for delineation of atypical Rett variants is reviewed.
openaire   +2 more sources

SARS-CoV-2 variants B.1.351 and P.1 escape from neutralizing antibodies

Cell, 2021
Markus Hoffmann   +2 more
exaly  

The roles of histone variants in fine-tuning chromatin organization and function

Nature Reviews Molecular Cell Biology, 2020
Sara Martire, Laura A Banaszynski
exaly  

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