Results 151 to 160 of about 9,152,470 (385)
Polyvisceral polycystic disease: a case study and review. [PDF]
Indumathi K+4 more
europepmc +1 more source
Identification of an N-terminal glycogen synthase kinase 3 phosphorylation site which regulates the functional localisation of polycystin-2 in vivo and in vitro [PDF]
PKD2 is mutated in 15% of patients with autosomal dominant polycystic kidney disease (ADPKD). Polycystin-2 (PC2), the PKD2 protein, is a nonselective Ca2 + -permeable cation channel which may function at the cell surface and ER. Nevertheless, the factors
Kane, M.E.+4 more
core +2 more sources
Polycystic Liver Disease: Pathophysiology, Diagnosis and Treatment
Luiz Fernando Norcia,1 Erika Mayumi Watanabe,2 Pedro Tadao Hamamoto Filho,3 Claudia Nishida Hasimoto,1 Leonardo Pelafsky,1 Walmar Kerche de Oliveira,1 Ligia Yukie Sassaki4 1Department of Surgery, São Paulo State University (Unesp), Medical School ...
Norcia LF+6 more
doaj
Exceptionally Large Kidneys in Autosomal Dominant Polycystic Disease in India. [PDF]
Shiza ST, Guttikonda J.
europepmc +1 more source
Uncovering anorexia nervosa in a biofeedback clinic for bowel dysfunction [PDF]
Biofeedback is a conservative treatment based on behavioural techniques, which can be used in the management of bowel dysfunction. This article reports the results of a retrospective review of the clinical notes of 87 female patients attending a ...
Chelvanayagam, Sonya+3 more
core +1 more source
(Poly)phenols constitute a source of natural therapeutic molecules capable of targeting angiogenesis in different scenarios. This review summarizes the current evidence of the role of (poly)phenols in modulating angiogenesis. The reader can find a compilation of preclinical and human investigations describing pro‐ and anti‐angiogenic effects of these ...
María Ángeles Ávila‐Gálvez+5 more
wiley +1 more source
Hyperinsulinemic hypoglycemia (HI) and congenital polycystic kidney disease (PKD) are rare, genetically heterogeneous disorders. The co-occurrence of these disorders (HIPKD) in 17 children from 11 unrelated families suggested an unrecognized genetic ...
O. R. Cabezas+45 more
semanticscholar +1 more source
Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery. [PDF]
Many families experience difficulty in talking about an inherited genetic condition that affects one or more of them. There have now been a number of studies identifying the issues in detail, however few have developed interventions to assist families ...
A McConkie-Rosell+52 more
core +4 more sources
Generational differences in associations between health conditions in young women and BMI categories
Abstract Objective The objective of this study was to investigate whether the associations between BMI categories and the age‐specific prevalence of health conditions common in young women differed across generations. Methods Data were from the Australian Longitudinal Study on Women's Health for participants born between 1973 and 1978 or 1989 and 1995 ...
Annette J. Dobson+2 more
wiley +1 more source