Articles with "gd1" as a keyword



Audiovestibular Findings in Gaucher Disease Types I and III: Evidence of Vestibular Involvement in GD1

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Published in 2025 at "Journal of Inherited Metabolic Disease"

DOI: 10.1002/jimd.70046

Abstract: Gaucher disease (GD), the most prevalent lysosomal storage disorder, is characterized by varying levels of systemic and neurological involvement. This study aims to investigate audiovestibular system involvement in patients with Gaucher disease type I (GD1)… read more here.

Keywords: gd1; gd3; disease; gaucher disease ... See more keywords

Multidisciplinary Study Based on Clinical, Electrophysiological and Psycological Evaluations Combined with Advanced Neuroimaging in Gaucher Disease Patients

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Published in 2019 at "Blood"

DOI: 10.1182/blood-2019-128143

Abstract: Gaucher Disease (GD) is an autosomal recessive metabolic disorder due to glucocerebrosidase deficit. There are three main clinical phenotypes: type I (GD1: non-neuronopathic form), characterized by a visceral involvement that can mimic a hematologic disease;… read more here.

Keywords: gd1; patients gd1; gd1 patients; gd1 gd3 ... See more keywords

Antibody reactions of horses against various domains of the EHV-1 receptor-binding protein gD1

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Published in 2024 at "PLOS ONE"

DOI: 10.1371/journal.pone.0301987

Abstract: Equid alphaherpesviruses 1 (EHV-1) and 4 (EHV-4) are closely related and both endemic in horses worldwide. Both viruses replicate in the upper respiratory tract, but EHV-1 may additionally lead to abortion and equine herpesvirus myeloencephalopathy… read more here.

Keywords: gd1; type specific; sera; antibody ... See more keywords