Results 81 to 90 of about 3,243 (180)

Genetic Polymorphisms of Prokineticins and Prokineticin Receptors Associated with Human Disease

open access: yesLife
Prokineticins (PKs) are low molecular weight proteins that exert their effects by binding to two seven-transmembrane G-protein-coupled receptors (prokineticin receptors, PKRs).
Roberta Lattanzi, Rossella Miele
doaj   +1 more source

Targeted Gene Panel Sequencing for Molecular Diagnosis of Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism [PDF]

open access: bronze, 2018
Ja Hye Kim   +7 more
openalex   +1 more source

Testicular ultrasound in a patient with Kallmann syndrome: A case report

open access: diamond, 2022
Daniela Donat   +5 more
openalex   +2 more sources

Profiling, Bioinformatic, and Functional Data on the Developing Olfactory/GnRH System Reveal Cellular and Molecular Pathways Essential for This Process and Potentially Relevant for the Kallmann Syndrome [PDF]

open access: gold, 2013
Giulia Garaffo   +10 more
openalex   +1 more source

Hypogonadotropic Hypogonadism Revisited

open access: yesClinics, 2013
Impaired testicular function, i.e., hypogonadism, can result from a primary testicular disorder (hypergonadotropic) or occur secondary to hypothalamic-pituitary dysfunction (hypogonadotropic).
Renato Fraietta   +2 more
doaj  

Kallmann's Syndrome [PDF]

open access: yesJournal of the Royal Society of Medicine, 1988
openaire   +2 more sources

KAL1基因突变的KS患者临床分析(附2例报告)

open access: yesZhongguo shiyan zhenduanxue, 2011
Kallmann综合征(Kallmann Syndrome,KS)又称促性腺激素分泌不足的性腺功能减退伴嗅觉丧失症,是一种先天性的遗传病。早期发现并及时给予激素替代治疗可使患者恢复性腺功能,部分患者可恢复生育力。本院在2008年收治两例KS患者,经KAL1基因分子筛查分析发现两例患者KAL1基因均有异常,现就两例KAL1基因突变的KS患者的临床表现及治疗进行报道如下。
李志   +5 more
doaj  

Delayed Puberty, Eroticism, and Sense of Smell, a Psychological Study of Economic and Social Consequences (Kallmann’s Syndrome): A Rare Case Report

open access: yesBiomolecular and Health Science Journal
Kallmann syndrome is defined as the association of hypogonadotropic hypogonadism and anosmia or hyposmia caused by abnormal migration of olfactory axons and neurons producing gonadotropin-releasing hormone.
Azlansyah Azlansyah   +6 more
doaj   +1 more source

Olfactory Agenesis in Kallmann Syndrome (KS) [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2015
Sahana Shetty   +3 more
doaj   +1 more source

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