Results 91 to 100 of about 119,031 (316)
Columbia Social Work Review, 2012 The goal of creating the idealized female form is neither new nor novel. Women have been altering their bodies for centuries. However, the focus recently has come onto the vagina – the most culturally value-laden of anatomical parts. This paper seeks to explore how historical representations and contemporary perceptions of the vagina have shaped ...
openaire +4 more sources
Expanded Phenotype Associated With an Intronic PPP1R12A Variant: A Case Report and Literature Review
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Autosomal dominant PPP1R12A‐related genitourinary and/or brain malformation syndrome is a recently described multisystem disorder caused by loss‐of‐function variants in the protein phosphatase 1 regulatory subunit 12a (PPP1R12A) gene. To date, 22 affected individuals have been reported with variable brain malformations and genitourinary ...
Emily M. Bland +4 more
wiley +1 more source
Neovagina Ileum Pada Agenesis Vagina Wanita Dewasa [PDF]
, 2019 Agenesis vagina adalah kondisi yang jarang terjadi. Sindrom Mayer-Rokitansky-Kuster-Hauser (MRKH) adalah diagnosa klinis yang paling sering ditemui ahli ginekologi dimana agenesis vagina terjadi akibat gangguan perkembangan duktus Mulleri.
Fauzi, Amir, Pratiwi, Ratih
core +1 more source
A Case of Multiple Mitochondrial Dysfunctions Syndrome 1 and Review of the Literature
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Multiple mitochondrial dysfunctions syndrome 1 (MMDS1, MIM #605711) due to NFU1 gene defects is an ultra‐rare autosomal recessive inborn error of metabolism associated with reduced function of NFU1 iron–sulfur cluster (ISC) scaffold protein.
Charles R. DiFalco +6 more
wiley +1 more source
Revista Colombiana de Ciencias Pecuarias, 2019 Background: Bovine campylobacteriosis is a venereal disease due to infection with Campylobacter fetus venerealis. It causes mainly reproductive failures that lead to considerable economic losses.
María Giobergia +4 more
doaj +1 more source
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT DNM1 encephalopathy is a rare autosomal dominant genetic condition characterized by a range of neurological and developmental manifestations. The typical phenotype is severe, including profound intellectual disability, treatment‐resistant epilepsy, ataxia, and structural brain abnormalities. However, milder presentations have increasingly been
Caroline Crain +6 more
wiley +1 more source
The Vagina Monologues 2014 [PDF]
, 2014 Poster promoting auditions for the 2014 performance of The Vagina ...
Student Women\u27s Association
core +1 more source
Relato de caso: melanoma primário de vagina [PDF]
, 2019 Introduction: Malignant melanoma of the vagina is a rare tumor with 0.46 cases per one million women per year and first described by Poronas in 1887. There are 500 cases reported.
Pinto, Marina Gontijo +4 more
core +2 more sources
Annals of Neurology, EarlyView.Objective Spinal muscular atrophy (SMA) is caused by deletions or mutations in the survival motor neuron 1 (SMN1) gene and subsequent reduction in the expression of survival motor neuron (SMN) protein. The disease is characterized by degeneration of α motor neurons and subsequent muscle atrophy.
Emma R. Sutton +4 more
wiley +1 more source