Results 41 to 50 of about 2,484,895 (385)

Postnatal clinical phenotype of five patients with Pallister–Killian Syndrome (tetrasomy 12p): Interest of array CGH for diagnosis and review of the literature

Molecular Genetics & Genomic Medicine, 2019
Background Pallister–Killian syndrome (PKS) is a rare sporadic disorder caused by tetrasomy of the short arm of chromosome 12. The main clinical manifestations are global developmental delay, intellectual disability, epilepsy, dysmorphic features ...
Amerh Salem Alqahtani, Audrey Putoux, Marie Noelle Bonnet Dupeyron, Maryline Carneiro, Laurence Lion‐Francois, Massimiliano Rossi, Hélène Tevissen, Caroline Schluth Bolard, Audrey Labalme, Gaetan Lesca, Marianne Till, Patrick Edery, Damien Sanlaville   +12 more
doaj   +1 more source

Giant hamartomatous polyp of the uterine cervix with heterologous mesenchymal tissue in a child: a case report

Journal of Medical Case Reports, 2021
Background Polyps of the uterine cervix are one of the most common benign hyperplastic lesions occurring in the female genital tract that usually arise from the endocervical canal and are believed to be the result of reactive changes due to long-standing
Esmatullah Esmat, Haider Ali Malakzai, Mujtaba Haidari, Ahmed Maseh Haidary, Merwaise Baha, Jamshid Abdul-Ghafar   +5 more
doaj   +1 more source

Somatisation and functional impairment in adolescents: longitudinal link with mothers' reactions [PDF]

, 2014
Adolescents' somatisation (i.e., the psychological tendency to experience and report multiple physical complaints for which no definite medical cause can be found; SOM) and functional impairment (i.e., all bothersome aftermath of somatisation; FI) were ...
Desoete, Annemie, Grietens, H, Hoppenbrouwers, K, Rousseau, S, Van Leeuwen, K, Vanderfaeillie, J   +5 more
core   +3 more sources

Support for healthy breastfeeding mothers with healthy term babies.

Cochrane Database of Systematic Reviews, 2012
BACKGROUND There is extensive evidence of important health risks for infants and mothers related to not breastfeeding. In 2003, the World Health Organization recommended infants be exclusively breastfed until six months of age, with breastfeeding ...
M. Renfrew, F. McCormick, A. Wade, Beverley Quinn, T. Dowswell   +4 more
semanticscholar   +1 more source

Acute lymphoblastic leukemia with clonal evolution due to delay in chemotherapy: A report of a case

eJHaem, 2022
Clonal evolution in acute leukemias is one of the most important factors that leads to therapeutic failure and disease relapse. Delay in therapeutic intervention is one of the reasons that leads toward clonal evolution.
Ahmed Maseh Haidary, Ramin Saadaat, Jamshid Abdul‐Ghafar, Soma Rahmani, Sarah Noor, Sahar Noor, Najla Nasir, Maryam Ahmad, Ahmad Shekib Zahier, Rohullah Zahier, Haider Ali Malakzai, Abdul Sami Ibrahimkhil, Samuel Sharif, Tawab Baryali, Inamullah Mohib, Abdul Hadi Saqib, Raja Zahratul Azma   +16 more
doaj   +1 more source

Developing Targeted Interventions to Advance Maternal Health in a Geographic Medicaid Accountable Care Organization: Lessons From the Implementation of Camden Delivers [PDF]

, 2017
Through the design and launch of Camden Delivers the Coalition developed targeted interventions within an ACO infrastructure to advance maternal health in a Medicaid-covered population. Key insights from this process include the need to:* Utilize data to
Margaret Hawthorne, Merck for Mothers, Molly Cherington, Natasha Dravid   +3 more
core  

The Potential Role of Mother-in-Law in Prevention of Mother-to-Child Transmission of HIV: A Mixed Methods Study from the Kilimanjaro Region, Northern Tanzania. [PDF]

, 2011
In the Kilimanjaro region the mother-in-law has traditionally had an important role in matters related to reproduction and childcare. The aim of this study was to explore the role of the mothers-in-law in prevention of mother-to-child transmission (PMTCT)
de Paoli, Marina Manuela, Engebretsen, Ingunn M S, Falnes, Eli Fjeld, Leshabari, Sebalda Charles, Moland, Karen Marie, Tylleskär, Thorkild   +5 more
core   +5 more sources

MET variants with activating N‐lobe mutations identified in hereditary papillary renal cell carcinomas still require ligand stimulation

Molecular Oncology, EarlyView.
MET variants in the N‐lobe of the kinase domain, found in hereditary papillary renal cell carcinoma, require ligand stimulation to promote cell transformation, in contrast to other RTK variants. This suggests that HGF expression in the microenvironment is important for tumor growth in such patients. Their sensitivity to MET inhibitors opens the way for
Célia Guérin, Audrey Vinchent, Marie Fernandes, Isabelle Damour, Agathe Laratte, Rémi Tellier, Gabriella O. Estevam, Jean‐Pascal Meneboo, Céline Villenet, Clotilde Descarpentries, James S. Fraser, Martin Figeac, Alexis B. Cortot, Etienne Rouleau, David Tulasne   +14 more
wiley   +1 more source

'I'm so much more myself now, coming back to work' - working class mothers, paid work and childcare [PDF]

, 2008
This paper explores the ways in which working class mothers negotiate mothering and paid work. Drawing on interviews with 70 families with pre-school children, we examine how caring and working responsibilities are conceptualised and presented in mothers’
Ball, Stephen, Braun, Annette, Vincent, Carol   +2 more
core   +3 more sources

Aberrant expression of nuclear prothymosin α contributes to epithelial‐mesenchymal transition in lung cancer

Molecular Oncology, EarlyView.
Nuclear prothymosin α inhibits epithelial‐mesenchymal transition (EMT) in lung cancer by increasing Smad7 acetylation and competing with Smad2 for binding to SNAI1, TWIST1, and ZEB1 promoters. In early‐stage cancer, ProT suppresses TGF‐β‐induced EMT, while its loss in the nucleus in late‐stage cancer leads to enhanced EMT and poor prognosis.
Liyun Chen, Chung‐Teng Wang, Jia‐Ming Chang, Ai‐Li Shiau, Gia‐Shing Shieh, Yau‐Lin Tseng, Yi‐Ting Yen, Tang‐Hsiu Huang, Li‐Hsin Cheng, Yu‐Chih Wu, Chao‐Liang Wu, Bing‐Hua Su, Pensee Wu   +12 more
wiley   +1 more source