Results 41 to 50 of about 157,574 (265)

Paternal Caffeine Exposure Programs Offspring Stress Vulnerability via Sperm Dlk1‐Dio3 Imprinting‐Directed Remodeling of a Novel Neural Circuit

Advanced Science, EarlyView.
The study elucidates that paternal preconception stress can drive offspring hyperresponsivity of the stress system via hypomethylation of a specific DNA region in sperm. This key link is confirmed in a cohort of prospective fathers: the epigenetic alteration is associated with elevated stress hormone levels.
Mengxi Lu, Gaole Dai, Sen Zhu, Shuai Zhang, Tingting Wang, Yuan Meng, Fang Yang, Xiaoyi Han, Hui Wang, Hao Kou, Dan Xu   +10 more
wiley   +1 more source

Running during pregnancy and postpartum, Part B: How does running-related advice and guidance received during pregnancy and postpartum affect women's running habits?

, 2022
Background: Women are unsure about the suitability and safety of running when pregnant and postpartum, with advice from medical professionals often conflicting.
James, Megan L., Donnelly, Gráinne M., Perkins, Joanna, Moore, Isabel S., Coltman, Celeste E., Brockwell, Emma   +5 more
core   +1 more source

Study on thermal responses and postpartum symptoms among postpartum women at a community hospital

Xi'an Gongcheng Daxue xuebao
To investigate the thermal response characteristics of postpartum women in air-conditioned rooms during summer and their relationship with postpartum symptoms, a community hospital was selected for research and thermal environment parameters were tested ...
WANG Lijuan, MOU Yaqin, CAO Chao, LIN Luyang, ZHANG Yijin   +4 more
doaj   +1 more source

Clinical, Behavioral and Neuroradiological Phenotype in an Italian Cohort of Patients With Xia Gibbs Syndrome: A Multicenter Cross‐Sectional Study and Systematic Literature Review

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli, Stefania Della Vecchia, Patrizia Bergonzini, Elisa Caramaschi, Elisabetta Spezia, Claudia Parenti, Simona Filomena Madeo, Laura Lucaccioni, Cavalleri Francesca, Marisa Pugliese, Federico Raviglione, Clara Colonna, Olga Calabrese, Ilaria Stanghellini, Maria Carmen Marongiu, Enrico Biagioni, Anna Rita Ferrari, Roberta Battini, Lorenzo Iughetti   +18 more
wiley   +1 more source

Factors associated with lack of postnatal care among Palestinian women: a cross-sectional study of three clinics in the West Bank

, 2008
Dhaher E, Mikolajczyk RT, Maxwell AE, Krämer A. Factors associated with lack of postnatal care among Palestinian women: a cross-sectional study of three clinics in the West Bank. BMC Pregnancy and Childbirth.
Krämer Alexander, Maxwell Annette E, Dhaher, Enas, Maxwell, Annette E., Mikolajczyk, Rafael T, Maxwell, Annette E, Krämer, Alexander ; https://orcid.org/, Annette E Maxwell, Alexander Krämer, Krämer, Alexander, Mikolajczyk Rafael T, Mikolajczyk, Rafael T., Dhaher Enas, Enas Dhaher, Rafael T Mikolajczyk   +14 more
core   +1 more source

Knowledge and Attitude Regard to Cord Blood of Early Postpartum Women after Donating Cord Blood or Storing Cord Blood. [PDF]

, 2009
PURPOSE: There is increasing necessity of using cord blood cell worldwide. In order to improve the effectiveness of cord blood's usage in Korea, the study of knowledge and attitude regarding cord blood is needed. METHODS: As descriptive correlation study,
박창기, 유지수
core   +1 more source

Spectrum of Congenital Anomalies in Myhre Syndrome—Insights Into Effects Brought by Altered TGF‐β Signaling via Gain‐of‐Function Variants in SMAD4

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is a rare genetic disorder characterized by progressive multisystem involvement. Gain‐of‐function missense heterozygous variants affecting the Ile500 residue and Arg496 residue of the SMAD4 gene are implicated in this condition.
Kawmadi Gunawardena, Alessandro De Falco, Deborah Osio, Eleanor Sherlock, Emma Kivuva, Erina Sasaki, Francis H. Sansbury, Nayana Lahiri, Patricia Foley, Sahar Mansour, Shane McKee, Tazeen Ashraf, Nicola Brunetti‐Pierri, Usha Kini   +13 more
wiley   +1 more source

Community-based adherence clubs for postpartum women on antiretroviral therapy (ART) in Cape Town, South Africa: a pilot study

BMC Health Services Research, 2020
Background With an increasing number of countries implementing Option B+ guidelines of lifelong antiretroviral therapy (ART) for all pregnant and breastfeeding women, there is urgent need to identify effective approaches for retaining this growing and ...
Allison Zerbe, Kirsty Brittain, Tamsin K. Phillips, Victoria O. Iyun, Joanna Allerton, Andile Nofemela, Cathy D. Kalombo, Landon Myer, Elaine J. Abrams   +8 more
doaj   +1 more source

Review of the Molecular and Developmental Basis of Myhre Syndrome, Bench Research

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome (MS) is a connective‐tissue disorder within the acromelic dysplasia spectrum. It is characterized by congenital craniofacial, skeletal, cutaneous anomalies, respiratory, cardiovascular along with intellectual disability, deafness, and progressive fibrosis.
Camille Viaut, Valerie Cormier‐Daire
wiley   +1 more source

Common perinatal mental disorders in northern Viet Nam: community prevalence and health care use. [PDF]

, 2010
OBJECTIVE: To establish the prevalence of common perinatal mental disorders their determinants, and their association with preventive health care use among women in one rural and one urban province in northern Viet Nam.
La, Buoi Thi, Jane Fisher, Buoi thi La, Fisher, Jane, Tuan Tran, Kelsi Kriitmaa, Thach Tran, Doreen Rosenthal, Kriitmaa, Kelsi, Tran, Thach, Rosenthal, Doreen, Tran, Tuan   +11 more
core   +1 more source