Results 161 to 170 of about 1,777,079 (364)

Male Sexual Dysfunction

open access: yesJournal of Andrology and Gynaecology, 2019
G. Egloff, I. Bender, Jasmin, Roemer
semanticscholar   +1 more source

Cystatin C as Biomarker for the Evaluation of Renal Outcome in AL Amyloidosis

open access: yesAmerican Journal of Hematology, EarlyView.
ABSTRACT Cystatin C (CysC) has emerged as a novel and potentially more reliable biomarker for the estimation of glomerular filtration in the general population in patients with various conditions. In AL amyloidosis, the current renal staging system and renal response criteria are based on proteinuria and creatinine‐based eGFR.
Foteini Theodorakakou   +18 more
wiley   +1 more source

Gut Microbiome Pilot Study of Patients With CHARGE Syndrome and Sibling Controls

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Difficulties with feeding and digestion are common in individuals with CHARGE syndrome. Animal models with CHD7 gene variants demonstrate abnormal gut innovation and dysmotility. Our pilot study evaluated whether individuals with CHARGE syndrome have differences in their gut microbiome compared to unaffected siblings.
Emily R. Chedrawe   +5 more
wiley   +1 more source

Prevalence of female sexual dysfunction and its correlated factors: a population based study

open access: yesPayesh, 2012
Objective (s): To determine the prevalence of sexual dysfunction and its effective factors in a community based study among reproductive aged women.Methods: In the present study, 784 married women, lived in urban area of Ghazvin, Golestan, Kermanshah and
Fahimeh Ramezani Tehrani   +4 more
doaj  

Sexual dysfunction in men undergoing fertility evaluation. [PDF]

open access: bronze, 2001
Geetha Ranga   +2 more
openalex   +1 more source

Children With 22.Q.11.2 Deletion Syndrome: Sleep‐Disordered Breathing and Management

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Patients with 22q11.2 deletion syndrome (22q11DS) are predisposed to obstructive sleep apnea (OSA) due to an abnormal craniofacial anatomy with pharyngeal hypotonia, retrognathia, micrognathia, and glossoptosis. The aim of the study was to describe the prevalence and management of OSA in a cohort of children with 22q11DS.
Domenico Paolo La Regina   +6 more
wiley   +1 more source

Extended Growth Curves for the Wolf‐Hirschhorn Syndrome (4p‐)

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Wolf‐Hirschhorn syndrome (WHS) is a rare, highly variable contiguous gene deletion syndrome caused by deletions of the distal portion of the short arm of chromosome 4. Individuals with this disorder have prenatal onset of poor growth of all dimensions, along with neurological manifestations, developmental disability, and distinctive facial ...
Amy R. U. L. Calhoun   +3 more
wiley   +1 more source

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