Results 61 to 70 of about 93,179 (152)

The Herlyn-Werner-Wunderlich (HWW) syndrome – A case report with radiological review

Radiology Case Reports, 2022
Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital anomaly of female urogenital tract involving combined mullerian duct anomalies and mesonephric duct malformation characterized by uterus didelphys, obstructed hemi-vagina and ipsilateral renal ...
Abdul Malik Hayat, MD, MPH, Khalid Rehman Yousaf, FCPS, Saman Chaudhary, FCPS, FRCR, Sohaib Amjad, FCPS   +3 more
doaj   +1 more source

Clinical and material degradations of intraocular lenses: A review [PDF]

, 2019
Purpose: To review the published scientific literature concerning clinical and material degradations of intraocular lenses after implantation in cataract surgery.
Hull, C., O’Brart, D. P. S., Stanojcic, N.   +2 more
core   +1 more source

Herlyn-Werner-Wunderlich syndrome: Case report

Revista de la Facultad de Medicina, 2021
Introduction: Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital malformation of the urogenital tract characterized by the triad of uterine didelphys, obstructed hemivagina, and ipsilateral renal agenesis, which is usually diagnosed after ...
Laura Catalina López-Alza, Mario Santiago Mesa-Espinel   +1 more
doaj   +1 more source

Herlyn Werner Wunderlich Syndrome with Hydrocolpos: A Case Report

Journal of Nepal Medical Association
Herlyn-Werner-Wunderlich Syndrome is a very rare congenital malformation of the urogenital tract involving both the Mullerian and Wolffian ducts characterized by the triad uterine diadelphys, obstructed vagina, and unilateral renal agenesis.
Saurav Sen Oli, Shova Sapkota, Rupa Bajagain, Rachana Saha, Suman Paudel   +4 more
doaj   +1 more source

The Werner syndrome protein is distinguished from the Bloom syndrome protein by its capacity to tightly bind diverse DNA structures. [PDF]

PLoS ONE, 2012
Loss of Werner syndrome helicase-exonuclease (WRN) or of its homolog Bloom syndrome helicase (BLM) results in different inherited disorders. Whereas Werner syndrome is characterized by premature onset of aging and age-associated diseases, Bloom syndrome ...
Ashwini Kamath-Loeb, Lawrence A Loeb, Michael Fry   +2 more
doaj   +1 more source

Long-term Symptomatic, Functional, and Work Outcomes of Carpal Tunnel Syndrome among Construction Workers [PDF]

, 2016
BACKGROUND: The long-term outcomes of carpal tunnel syndrome (CTS) including symptoms, functional status, work disability, and economic impact are unknown. METHODS: We conducted a retrospective study of 234 active construction workers with medical claims
Amick, Armstrong, Cagle, Dale, Daniell, Daniell, DeStefano, Dong, Foley, Forde, Franklin, Franzblau, Gardner, Gardner, Gimeno, Glazner, Gorsche, Hudak, Ilmarinen, Katz, Keith, Kuorinka, Levine, Lipscomb, Louie, Manktelow, Padua, Pensy, Probst, Resende, Rosecrance, Salerno, Spector, Turner, Ware, Welch, Wellman   +36 more
core   +2 more sources

Mutations Involved in Premature-Ageing Syndromes

The Application of Clinical Genetics, 2021
Fabio CoppedèDepartment of Translational Research and of New Surgical and Medical Technologies, University of Pisa, Pisa, ItalyCorrespondence: Fabio CoppedèDepartment of Translational Research and of New Surgical and Medical Technologies ...
Coppedè F
doaj  

A novel ZRS variant causes preaxial polydactyly type I by increased sonic hedgehog expression in the developing limb bud. [PDF]

, 2020
PurposePreaxial polydactyly (PPD) is a common congenital hand malformation classified into four subtypes (PPD I-IV). Variants in the zone of polarizing activity regulatory sequence (ZRS) within intron 5 of the LMBR1 gene are linked to most PPD types ...
Ahituv, Nadav, Chen, Tao, Gao, Bo, Li, Quan-Zhen, Li, Yongyong, Lian, Chengjie, Liao, Zhiheng, Malik, Sajid, Mohan, Chandra, Sharma, Swarkar, Su, Deying, Su, Peiqiang, Wang, Tingting, Xing, Chao, Xu, Caixia, Yan, Mei, Yang, Xiaoming, Zhong, Dongmei, Zhou, Hang, Zhou, Taifeng   +19 more
core  

Root enhancement in cytokinin-deficient oilseed rape causes leaf mineral enrichment, increases the chlorophyll concentration under nutrient limitation and enhances the phytoremediation capacity [PDF]

, 2019
Background Cytokinin is a negative regulator of root growth, and a reduction of the cytokinin content or signalling causes the formation a larger root system in model plants, improves their growth under drought and nutrient limitation and causes ...
Gerdemann-Knörck, Maria, Nehnevajova, Erika, Novák, Ondřej, Ramireddy, Eswarayya, Schmülling, Thomas, Stolz, Andrea, Strnad, Miroslav   +6 more
core   +3 more sources

Identification and characterization of an inhibitory fibroblast growth factor receptor 2 (FGFR2) molecule, up-regulated in an Apert Syndrome mouse model [PDF]

, 2011
AS (Apert syndrome) is a congenital disease composed of skeletal, visceral and neural abnormalities, caused by dominant-acting mutations in FGFR2 [FGF (fibroblast growth factor) receptor 2].
Anderson, Beenken, Bochukova, Burgar, Celli, Cohen, De Moerlooze, Duan, Duchesne, Ezzat, Fairbanks, Hajihosseini, Hajihosseini, Hajihosseini, Hajihosseini, Hajihosseini, Hanneken, Ibrahimi, Jang, Jang, Jang, John K. Heath, Jones, Kawano, Klein, Kuro-o, Lee M. Wheldon, Lewis, Maquat, McKeehan, Mendell, Meyers, Miki, Mohammad K. Hajihosseini, Muhlemann, Naila Khodabukus, Naski, Nelson, Oldridge, Peters, Polanska, Ricol, Saito, Sekine, Slaney, Smith, Susannah J. Patey, Takaishi, Tanimoto, Terada, Terence G. Smith, Tsang, Tsukuno, Werner, Wheldon, Wilkie, Yamaguchi, Zhang   +57 more
core   +3 more sources