Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Miriam Blumenkrantz"'
Autor:
Lionel Buré, Louis-Martin Boucher, Miriam Blumenkrantz, Stefan Schob, Pierre Lafaye de Micheaux, Caroline Reinhold, Benoit Gallix
Publikováno v:
PLoS ONE, Vol 12, Iss 8, p e0182169 (2017)
Lymphadenopathy continues to be a common problem to radiologists and treating physicians because of the difficulty in confidently categorizing a node as being benign or malignant using standard diagnostic techniques. The goal of our research was to a
Externí odkaz:
https://doaj.org/article/7ee99932aa114546973e4a8da39723c7
Autor:
Chantal Bernard, Corinne Antignac, Nancy Braverman, Martin Bitzan, Miriam Blumenkrantz, Indra R. Gupta, Vincent Morinière, Marie Claire Gubler, K. Bridget Brosnihan, Ahmed Alfares, Avi Saskin, Isabelle De Bie
Publikováno v:
European Journal of Medical Genetics. 62:254-258
Renal tubular dysgenesis (RTD) is a developmental abnormality of the nephron characterized by fetal anuria, oligohydramnios, and severe postnatal hypotension. Genetic forms have an autosomal recessive inheritance and are caused by mutations in genes
Autor:
Pierre Lafaye de Micheaux, Lionel Bure, Benoit Gallix, Stefan Schob, Louis-Martin Boucher, Miriam Blumenkrantz, Caroline Reinhold
Publikováno v:
PLoS ONE, Vol 12, Iss 8, p e0182169 (2017)
PLoS ONE
PLoS ONE
Lymphadenopathy continues to be a common problem to radiologists and treating physicians because of the difficulty in confidently categorizing a node as being benign or malignant using standard diagnostic techniques. The goal of our research was to a
Autor:
Serge Mayrand, Veronique D. Morinville, Sherif Emil, Jean-Martin Laberge, Miriam Blumenkrantz, Van-Hung Nguyen, Abdullah Alshehri, Sherif Elkady
Publikováno v:
Journal of Pediatric Surgery. 49:1353-1359
We previously demonstrated feasibility, safety, and a reproducible histologic bulking effect after injection of dextranomer hyaluronic acid copolymer (DxHA) into the gastroesophageal junction of rabbits. In the current study, we investigated the pote
Publikováno v:
Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery. 156(2)
Onabotulinum toxin A (OBTXA) is an effective treatment for drooling. Our objective was to determine if there are histologic changes in the submandibular glands (SMGs) after repetitive OBTXA injections. The study included blinded histologic analysis a
Autor:
Fady Gaied, Robert Baird, Miriam Blumenkrantz, Chantal Bernard, Jean-Martin Laberge, Van-Hung Nguyen, Sherif Emil, Kenneth Shaw, Andrea Lo, Pramod Puligandla
Publikováno v:
Journal of Surgical Research. 177:123-126
Introduction The definition and treatment of gangrenous appendicitis are not agreed upon. We performed a prospective study in children to evaluate an objective definition of gangrenous appendicitis, as well as associated bacteriology, histopathology,
Publikováno v:
Clinical Nuclear Medicine. 35:872-874
Dermatopathic lymphadenitis (also known as lipomelanotic reticulosis, or Pautrier–Woringer disease) is a rare type of benign lymphatic hyperplasia associated with a variety of exfoliative or eczematoid type inflammatory erythrodermas. The axillary
Autor:
Miriam Blumenkrantz, Jean-Martin Laberge, Chantal Bernard, Fady Gaied, Van-Hung Nguyen, Veronique D. Morinville, Sherif Emil, Kathryn Martin
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 58(5)
Objective: The outcomes of fundoplication for gastroesophageal reflux disease are suboptimal in many children, and alternatives are clearly needed. Dextranomer hyaluronic acid (DxHA) copolymer, an agent with proven efficacy in vesicoureteral reflux,
Autor:
Miriam Blumenkrantz, Helena Evangeliou, Veronique D. Morinville, Suzanne MacDonald, Jean-Martin Laberge
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 59(2)
Publikováno v:
Pediatric surgery international. 29(7)
Mesenchymal hamartoma of the chest wall is a rare, benign chondro-osseous tumor of the bone. Although it most commonly presents at birth or soon after, prenatal detection is rare. We report a case of prenatally detected mesenchymal hamartoma, and pro