Results 91 to 100 of about 14,959 (189)

Human diseases caused by homozygous PTH1R mutations. [PDF]

open access: yesFront Endocrinol (Lausanne)
Portales-Castillo I   +3 more
europepmc   +1 more source

Use of Artificial Intelligence-Based Software to Aid in the Identification of Ultrasound Findings Associated With Fetal Congenital Heart Defects. [PDF]

open access: yesObstet Gynecol
Lam-Rachlin J   +27 more
europepmc   +1 more source

Gardella/exposing: the shop and the stand

open access: yesFestival dell'Architettura Magazine, 2018
Federico Marcolini
doaj   +1 more source

Gardella/the transmission: photography between “iconization” and evidence

open access: yesFestival dell'Architettura Magazine, 2018
Sebastiano Marconcini
doaj   +1 more source

Circulating cell-free RNA signatures for the characterization and diagnosis of myalgic encephalomyelitis/chronic fatigue syndrome. [PDF]

open access: yesProc Natl Acad Sci U S A
Gardella AE   +9 more
europepmc   +1 more source

Artificial Intelligence for the Detection of Fetal Ultrasound Findings Concerning for Major Congenital Heart Defects. [PDF]

open access: yesObstet Gynecol
Zelop CM   +23 more
europepmc   +1 more source

Unmasking the role of the occipital lobe in epilepsy with eyelid myoclonia. [PDF]

open access: yesEpilepsia
Ricci E   +16 more
europepmc   +1 more source

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