Results 141 to 150 of about 53,350 (292)

Alcohol and hypogonadism

Gastroenterology, 1981
C, Balabaud, F, Magne, J, Saric, P, Bioulac   +3 more
openaire   +2 more sources

Biochemical profiling and symptomatology of androgen deficiency in males with cluster headache: A prospective case–control study

Headache: The Journal of Head and Face Pain, EarlyView.
Abstract Objectives/Background Cluster headache (CH) has historically been considered a male‐dominated disorder, suggesting a role for androgens in its pathophysiology. We aimed to evaluate hormone profiles and symptoms of androgen deficiency in CH.
Willemijn C. Naber, Roemer B. Brandt, Mariël Leon Morales‐Grooters, Ronald van der Wal, Sjoerd A. A. van den Berg, Jelle J. Goeman, Antoinette Maassen van den Brink, Rolf Fronczek   +7 more
wiley   +1 more source

Bone health in adults with non‐ambulatory neuromuscular disorders: scoping review of risk factors, diagnosis and management

Internal Medicine Journal, EarlyView.
Abstract Background Non‐ambulatory adults have an increased risk of osteoporosis and fractures due to reduced weight‐bearing and diminished neuromuscular stimulation, resulting in substantial morbidity and mortality. Aims This scoping review aimed to systematically evaluate risk factors, diagnostic indicators and management strategies for optimising ...
Thomas Bailey, Carolyn Droste, John A. Eisman, Steven G. Faux, Arnagretta Hunter   +4 more
wiley   +1 more source

When to consider an inborn error of immunity: clues for physicians

Internal Medicine Journal, EarlyView.
Abstract The term inborn errors of immunity (IEIs) refers to the rapidly expanding group of genetic disorders causing dysregulation of the immune system. With improved genetic testing in recent years, the number of defined IEIs and their range of phenotypic presentations has grown vastly, with more than 550 IEIs now described.
Meera Thangarajah, Lucinda J. Berglund
wiley   +1 more source

Aligning clinical care with consumer priorities: an adult cystic fibrosis centre experience of co‐designing a model of care

Internal Medicine Journal, EarlyView.
Abstract Cystic fibrosis (CF) is a multi‐system genetic condition, and CF modulator therapies have transformed health outcomes promising improved longevity. Our aim was to co‐design and implement a nested endocrine and metabolic model of care called CF Endocrine for adults with CF that aligned with consumer and healthcare provider priorities and ...
Shanal Kumar, Vanessa Moore, Daniel Smith, Angela Matson   +3 more
wiley   +1 more source

Bone mineral density in adolescents and young women with hypogonadism: a DXA-based comparative analysis. [PDF]

J Turk Ger Gynecol Assoc
Kurtoğlu N, Hayırlıoğlu N.
europepmc   +1 more source

Reversal of idiopathic hypogonadotropic hypogonadism [PDF]

Background: Idiopathic hypogonadotropic hypogonadism, which may be associated with anosmia (the Kallmann syndrome) or with a normal sense of smell, is a treatable form of male infertility caused by a congenital defect in the secretion or action of ...
Pearce SH, Falardeau J, Dwyer A, Quinton R, Hayes FJ, Hughes VA, Boepple P, Pitteloud N, Lee H, Crowley WF, Cole LW, Raivio T   +11 more
core  

American Geriatrics Society Position Statement: Advancing the Healthcare of Lesbian, Gay, Bisexual, Transgender, Queer, Intersex, and More Older Adults

Journal of the American Geriatrics Society, EarlyView.
ABSTRACT In the decade since the American Geriatrics Society (AGS) released a position statement on Care of Lesbian, Gay, Bisexual, and Transgender Older Adults, we have seen significant progress toward achieving equal health and civil rights for lesbian, gay, bisexual, transgender, queer, intersex, and more (LGBTQI+) individuals.
Carl H. Burton, Maria H. van Zuilen, Chelsea Namahana Wong, Angela Primbas, Michael Danielewicz, Timothy W. Farrell, Rohin Aggarwal, Carl G. Streed Jr., Aruna V. Josyula, Reena Karani, Alexia Mary Torke, Bronwyn Keefe, Joseph Shega, Noelle Marie Javier   +13 more
wiley   +1 more source

A 5-Year Outcome of Closed Reduction and Screw Fixation for an Atypical Slipped Capital Femoral Epiphysis Associated with Hypogonadism: A Case Report. [PDF]

J Orthop Case Rep
Lingaiah P, Rambabu L, Venkataramana K, Nataraj AR.   +3 more
europepmc   +1 more source

CHARGE Syndrome: A Narrative Review and Update on Diagnosis, Assessment and Management

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT Background CHARGE syndrome (CS) is a rare multisystemic genetic condition caused by a pathogenic variant in the DNA‐binding protein‐7 CHD7 gene. The condition affects the development of neural crest cells, which give rise to craniofacial structures, cranial nerves, ears, eyes and the heart, resulting in diverse and complex clinical features ...
Eleni M. van Gelder, Suzanna E. L. Temple, Niall Jefferson, David Brown, Kasee Stratton‐Gadke, Madelene Rich, Steve Rose, Kim Blake   +7 more
wiley   +1 more source