Results 241 to 250 of about 4,075,610 (383)

Sleep disorders in cancer: interactions and intrinsic links. [PDF]

open access: yesFront Oncol
Han C   +5 more
europepmc   +1 more source

Etiology and treatment of intrinsic circadian rhythm sleep disorders

open access: hybrid, 1999
Scott S. Campbell   +4 more
openalex   +1 more source

Sleep-Disordered Breathing in Alcoholics [PDF]

open access: green, 1999
Michael S. Aldrich   +2 more
openalex   +1 more source

Trisomy 5p: Long Recognized, Rarely Published‐ Three New Cases and Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Complete trisomy 5p is a rare chromosomal disorder caused by a duplication of the short arm of chromosome 5. Current data suggest that complete trisomy 5p presents as a distinct clinical syndrome including but not limited to seizures, developmental delays, facial dysmorphisms, failure to thrive, and recurrent respiratory infections.
Gabriela J. Kim   +2 more
wiley   +1 more source

Commentary on “Transient intracranial pressure elevations (B waves) associated with sleep apnea”: the neglected role of cyclic alternating pattern

open access: yesFluids and Barriers of the CNS
Carlotta Mutti   +6 more
doaj   +1 more source

Publisher Correction: Circadian lipid and hepatic protein rhythms shift with a phase response curve different than melatonin

open access: yesNature Communications, 2022
Brianne A. Kent   +6 more
doaj   +1 more source

Genetic Studies in the Sleep Disorder Narcolepsy [PDF]

open access: hybrid, 1998
Hiroshi Kadotani   +2 more
openalex   +1 more source

Case Series of Nizon‐Isidor Syndrome by Heterozygous Variants in MED12L With Further Evidence of Mitotic Instability in One Case With Diploid–Triploid Mosaicism

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Nizon‐Isidor syndrome is a rare disorder caused by heterozygous variants in MED12L, with only eight documented cases in the literature. Here, we present three additional cases of this syndrome. Proband 1 was a 7‐year‐old female who presented with developmental delay, right‐leg hemihypertrophy, laryngeal cleft, esotropia, abnormal skin ...
Russell Stewart   +336 more
wiley   +1 more source

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