Results 101 to 110 of about 2,719 (152)

Autosomal dominant Riggs-type congenital stationary night blindness with fundus sheen and retinal atrophy due to a novel GNAT1 p.Gln200Arg variant. [PDF]

open access: yesDoc Ophthalmol
Chou JJ   +7 more
europepmc   +1 more source

Longitudinal Evaluation of Neurological and Sensory Changes in Gaucher Disease: A Prospective Observational Cohort Study (SENOPRO). [PDF]

open access: yesMed Sci (Basel)
Cerulli Irelli E   +14 more
europepmc   +1 more source

Multiple Evanescent White Dot Syndrome After mRNA COVID-19 Vaccination. [PDF]

open access: yesCureus
Sakamoto R   +6 more
europepmc   +1 more source

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