Results 131 to 140 of about 1,533,449 (332)

Repeat Expansions in PLIN4 Cause Autosomal Dominant Vacuolar Myopathy With Sarcolemmal Features

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective We aim to describe and characterize two unrelated Spanish families suffering from an autosomal dominant autophagic vacuolar myopathy caused by repeat expansions in PLIN4. Methods We evaluated the clinical phenotype and muscle imaging, and performed a genetic workup that included exome sequencing, muscle RNAseq, and long‐read genome ...
Laura Llansó   +17 more
wiley   +1 more source

Editorial: Behavior and Welfare of the Individual Within Large, Commercially-Relevant Groups

open access: yesFrontiers in Veterinary Science, 2021
Michael J. Toscano   +2 more
doaj   +1 more source

Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco   +18 more
wiley   +1 more source

Rabbits

open access: yes, 1999
Es una guía práctica para los amantes de animales de compañía que quieran saber cómo cuidar un conejo. Hay mucha información sobre cómo elegirlo, el equipo que va a necesitar y la forma de limpiar su conejera. También hay consejos sobre aseo personal así como los aspectos típicos de su comportamiento.
Patchett, Fiona, Fox, Christyan (il.)
openaire   +1 more source

Tuberculous Granulomas Are Hypoxic in Guinea Pigs, Rabbits, and Nonhuman Primates

open access: yesInfection and Immunity, 2008
Barry Iii Cho   +17 more
semanticscholar   +1 more source

Growth Differentiation Factor 15 Elevation in the Central Nervous System Is Associated With Failure to Thrive in Alexander Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Alexander disease (AxD) is a severe neurodegenerative disorder caused by gain‐of‐function mutations in the gene for GFAP, which lead to protein aggregation and a primary astrocytopathy. Symptoms vary, but failure to thrive (FTT) and frequent emesis are common and cause significant morbidity. Here we investigate GDF15, a member of the
Tracy L. Hagemann   +6 more
wiley   +1 more source

Conditions which eliminate Inflammation to Homografts in Rabbits [PDF]

open access: bronze, 1958
Richard H. Andresen   +3 more
openalex   +1 more source

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