Results 51 to 60 of about 8,787 (248)

Complications of Cushing's syndrome: state of the art [PDF]

open access: yes, 2016
Cushing's syndrome is a serious endocrine disease caused by chronic, autonomous, and excessive secretion of cortisol. The syndrome is associated with increased mortality and impaired quality of life because of the occurrence of comorbidities.
Biller, Beverly M. K   +5 more
core   +1 more source

Characterisation of Chemical Constitutes and Spermatogenic Activity of Ushir (Vetiveria Zizanioides Linn) versus Ikshu (Saccharum Officinarum Linn) in Male Wistar Rats: A Research Protocol [PDF]

open access: yesJournal of Clinical and Diagnostic Research
Introduction: In men, infertility may results from impaired sperm quality, quantity and abnormalities. In Ayurveda, there are various herbal medicines that are stated to possess effective aphrodisiac (Vajikarana) properties and purification of the semen (
Akshay Sudhir Pargaonkar   +3 more
doaj   +1 more source

Screening of mutations and polymorphism in CFRT gene in men infertile due to oligo- or azospermia [PDF]

open access: yesSrpski Arhiv za Celokupno Lekarstvo, 2002
We concluded that CFTR gene plays a role in the etiology of obstructive azoospermia and that it also could be involved in same cases of impaired spermatogenesis and sperm maturation.
Kušić Jelena S.   +4 more
doaj   +1 more source

Engineered nanoparticles potentials in male reproduction

open access: yesAndrology, Volume 13, Issue 4, Page 694-705, May 2025.
Abstract Background The escalating prevalence of fertility problems in the aging population necessitates a comprehensive exploration of contributing factors, extending beyond environmental concerns, work‐related stress, and unhealthy lifestyles. Among these, the rising incidence of testicular disorders emerges as a pivotal determinant of fertility ...
Feifei Zhao   +8 more
wiley   +1 more source

A procedure to detect 6 basic STSs and 11 extended STSs in the AZF region using multiplex PCR

open access: yesVietnam Journal of Science, Technology and Engineering, 2022
Microdeletions of Y chromosomes frequently occur in 3 subregions of the AZF, namely, AZFa, AZFb, and AZFc, with 6 basic STS marker sequences, which are sY84, sY86 (AZFa), sY127, sY134 (AZFb), and sY254, sY255 (AZFc). According to EAA/EMNQ guidelines, 11
Thi Lan Anh Luong   +3 more
doaj   +1 more source

The role and implication of platelet‐rich plasma in male factor infertility: A systematic review of human studies

open access: yesAndrology, EarlyView.
Abstract Background Cryopreservation causes sperm injury and the success of surgical sperm retrieval (SSR) for azoospermic men is just over half depending on the cause of azoospermia. The role of autologous platelet‐rich plasma (PRP) in male factor infertility (MFI) is unclear. Objective To conduct a systematic review of the role of PRP in MFI focusing
Karl H. Pang
wiley   +1 more source

A survey of chromosome anomalies in Malta [PDF]

open access: yes, 1989
433 individuals referred for chromosome analysis between 1983 and 1987 were included in the survey. Among individuals with dysmorphic features or congenital anomalies 42% of babies referred in the neonatal period and 12 to 30% of individuals in older age
Cuschieri, Alfred, Gauci, Sandra
core  

A case study of Shukra Kshaya w.s.r. to Oligospermia [PDF]

open access: yes, 2023
Male infertility is primarily caused by low sperm count (oligospermia) and reduced sperm motility (asthenospermia), which can be linked to Shukravaha Srotas Dushti and is an issue of global dimensions.
Jitendra Sankhala   +3 more
core   +2 more sources

Influence of Arginine on Oligospermia

open access: yesExperimental Biology and Medicine, 1947
Summary1. Eighteen infertile men with oligospermia received 1.8-2.7 g of arginine and minimal amounts of lysine, pyridoxine, and tryptophane in tablet form for 8 months.2. The tendency for sperm concentration to increase was as great in the untreated group as in the treated groups.3. Although no pregnancies occurred in the treated groups, 2 pregnancies
openaire   +3 more sources

Aarskog Syndrome: Deep Phenotyping and Genomic Landscape of a New Cohort Including Adult Patients

open access: yesClinical Genetics, EarlyView.
This study presents the deep phenotyping data of 14 new Aarskog‐Scott syndrome patients with molecular confirmation. ABSTRACT Aarskog‐Scott syndrome (AAS, MIM#305400) is an X‐linked disorder characterized by recognizable facial features, short stature, and genitourinary and skeletal malformations.
Gozde Tutku Turgut   +7 more
wiley   +1 more source

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