Results 151 to 160 of about 295,957 (265)

Improving access to fertility treatment in Asia Pacific: consensus from an expert forum. [PDF]

Front Reprod Health
Abat MAG, Armstrong H, Chen MJ, Fatemi H, Hung HS, Nakagawa K, Pannu NS, Petrova A, Pistollato M, Pruksananonda K, Lee JR, Yong TT.   +11 more
europepmc   +1 more source

Rüdin's Unpublished Family Study From the Early 1920s: “On the Inheritance of Manic‐Depressive Insanity”

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Ernst Rüdin, an important and controversial figure in the history of psychiatric genetics, published only one major empirical study on siblings of dementia praecox (DP) probands in 1916. He conducted a parallel study of siblings of probands with manic‐depressive insanity (MDI), but the resulting monograph, written in the early 1920s, was left ...
Kenneth S. Kendler, Astrid Klee
wiley   +1 more source

Unmet patient needs and information gaps in fertility counseling for persons living with HIV/AIDS: Evidence from Ghana. [PDF]

PLOS Glob Public Health
Boadi PA, Dzramado VL.
europepmc   +1 more source

Fertility 2015 [PDF]

Human Fertility, 2015
openaire   +2 more sources

Therapy for Myhre Syndrome: Goals, Misconceptions, and Current Agents

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre Syndrome (MYHRS, MIM #139210) is a rare, multisystem connective tissue disorder caused by recurrent heterozygous gain‐of‐function pathogenic variants in the SMAD4 gene, a key player in TGF‐β signaling and a regulator of extracellular matrix homeostasis.
Alessandro De Falco, Alfonso Manuel D'Alessio, Nicola Brunetti‐Pierri   +2 more
wiley   +1 more source

Fertility Preservation for Patients with Malignant Disease. Guideline of the DGGG, OEGGG and SGGG (S2k-Level, AWMF Registry No. 015/082, May 2025). [PDF]

Geburtshilfe Frauenheilkd
Lotz L, Kliesch S, Baston-Buest D, Schüring A, Balcerek M, Bartsch B, Baumann R, Beckmann M, Behringer K, Borgmann-Staudt A, Böttcher B, Corradini S, Cremer W, Dinkel A, Diesch-Furlanetto T, Frenz S, Germeyer A, Goeckenjan M, Hepp V, Hetzer F, Jarisch A, Kentenich H, Knuth UA, Korell M, Köhn FM, Bender-Liebenthron J, Lindel K, Leszinski GS, Lux M, Meißner J, Micke O, Müller A, Nawroth F, Nordhoff V, Oppelt P, Reisch N, Reiser E, Reschke F, Rink A, Sahi A, Sänger N, Soave A, Roxana S, Sigg C, Sikora M, Tauchert S, Thorn P, Weberschock T, Wimberger P, Wischmann T, Würstlein R, von Wolff M, Dittrich R.   +52 more
europepmc   +1 more source

Unveiling a New Link: Cholesterol Deficiency in Smith–Lemli–Opitz and Niemann–Pick C as a Driver of Ciliopathies

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The ciliopathies are a group of genetic disorders caused by defective function of either the primary cilia (a large number) or the motile cilia (a much smaller number). These have been defined as diseases with mutations in genes encoding individual ciliary or cilia‐associated proteins.
Robert P. Erickson, Maria Teresa Fiorenza   +1 more
wiley   +1 more source

Association between epidural analgesia experience and future fertility intention in China: a national cross-sectional study. [PDF]

BMJ Open
Yu J, Gao Y, Liu T, Ma X, Wu C, Leung CK, Huang J, Akinwunmi BO, Liang S, Fu W, Liu X, Zhang CJP, Wu Y, Fekadu G, Ming WK.   +14 more
europepmc   +1 more source

How Do I Answer This? A Queer Critique of Australian Census Forms and the Reification of Cisheteronormative Families

Australian Journal of Social Issues, EarlyView.
ABSTRACT This paper presents a critical examination of Australia's 2021 household, individual and interviewer census forms. Using a form‐led analysis, this research scrutinises the underlying cisheteronormative logic that implicitly shapes the Census process, from data collection to distribution of findings.
Xavier Mills, Sal Clark
wiley   +1 more source

Zebrafish and CRISPR—A synergistic approach to decipher and cure human diseases

Animal Models and Experimental Medicine, EarlyView.
Zebrafish, with high genetic homology to humans, serves as a powerful vertebrate model for disease modeling and drug discovery. Integration of CRISPR/Cas9 technology enables precise genome editing, facilitating the development of translational models for human diseases.
Manikandan Sivaprakasam, Aashika Raagavi Jeanpierre, Salma Mohammed, Rajesh Srinivasan, Aman Kumar Mohanty   +4 more
wiley   +1 more source