Results 41 to 50 of about 163,414 (205)

Trombose de seio sigmoide secundária a fístula liquórica espontânea para osso temporal: um relato de caso

Clinical and Biomedical Research, 2022
A fístula liquórica para o osso temporal constitui um evento raro que decorre da comunicação anormal entre o espaço subaracnóideo e as células da mastoide, permitindo que o líquido cefalorraquidiano flua para as porções pneumatizadas do osso temporal ...
Flávia Rauber Felkl, Letícia Lemes Gai, Marina Paese Pasqualini, Paulo Moacir Mesquita Filho, Juliana Sato Hermann, Diego Rodrigo Hermann, Fábio Pires Santos   +6 more
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Uso de la ecografía como apoyo de la técnica de redireccionamiento de la aguja en el dolor de la fistula arteriovenosa durante la hemodiálisis

Enfermería Nefrológica, 2015
Es indudable que el acceso vascular no sólo es uno de los elementos clave para poder llevar a cabo el tratamiento sustitutivo renal con hemodiálisis sino que representa una de las principales causas de morbilidad, hospitalización y coste en los enfermos
Antonio López González, Constantino Fernández Rivera, Lorena Díaz Rodríguez, Mª del Carmen Ornosa Agra   +3 more
doaj   +1 more source

Artificial Intelligence–Based Surgical Phase Analysis Enables Objective Assessment of Surgeon Skill in Robotic Distal Gastrectomy: A Multicenter Study

Annals of Gastroenterological Surgery, EarlyView.
ABSTRACT Aim Artificial intelligence (AI)–based surgical video analysis can automate time‐consuming manual assessments and enable objective characterization of surgical workflows. We aimed to construct a large, multicenter, fully annotated dataset of robotic distal gastrectomy (RDG) videos and evaluate the feasibility and performance of an AI model for
Masaru Komatsu, Daichi Kitaguchi, Yoichi Ninomiya, Yuya Takabe, Mitsumasa Yoshida, Masahiro Yura, Nobuyoshi Takeshita, Takahiro Kinoshita, Masaaki Ito   +8 more
wiley   +1 more source

The Homozygous p.(Arg215Ter) Variant in XRCC2 Is Associated With Atypical Fanconi Anemia Without Major Hematological Abnormalities in Childhood

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli, Giulia Bruna Marchetti, Maria Iascone, Maria Grazia Patricelli, Sara Giangiobbe, Gabriella Cinzia Pozzobon, Miriam Nella Savini, Fabio Giglio, Alessandro Aiuti, Paola Carrera, Francesca Ferrua, Angela Peron   +11 more
wiley   +1 more source

Fístula gastrocutánea espontánea

Cirugía del Uruguay, 1974
Exponemos un caso que creemos presente un doble interés. Por un lado la presentación de una fístula gastrocutánea espontánea, hecho de extrema rareza.
Vladimir Guicheff, Raul Villagran, Juan Favat, Sergio Ramoe   +3 more
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Clinical Outcomes and Patient Experiences With Celiprolol Therapy in Vascular Ehlers–Danlos Syndrome: The First Non‐European Cohort

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Vascular Ehlers–Danlos syndrome (vEDS) is a hereditary connective tissue disorder caused by heterozygous pathogenic variants in COL3A1. European studies have shown that celiprolol may reduce the risk of life‐threatening vascular events, but outcomes in non‐European populations and the therapy's psychological impact remain unclear. We conducted
Megumi Furuhata‐Yoshimura, Tomomi Yamaguchi, Tomoki Kosho   +2 more
wiley   +1 more source

Fístula biliar interna espontánea

Cirugía del Uruguay, 2020
Presentado en sesión de 22 de abril de ...
Luis M Bosch del Marco
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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, Amber Nakar Weinstein, Eric C. Kao, Xiaonan Zhao, Monika Weisz‐Hubshman   +4 more
wiley   +1 more source

Co‐Occurring Non‐Cardiac Congenital Anomalies Among Cases With Congenital Heart Defects

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cases with congenital heart defects (CHD) often have other associated anomalies. The aim of this investigation was to assess the prevalence and the types of co‐occurring anomalies in CHD in a well‐defined population. The anomalies co‐occurring with CHD were ascertained in all live births, stillbirths and terminations of pregnancy for fetal ...
Claude Stoll, Yves Alembik, Marie‐Paule Roth   +2 more
wiley   +1 more source

Fístula cutánea: un caso clínico Cutaneous fistula: a case report

Revista de la Asociación Odontológica Argentina, 2016
Resumen Objetivo: Diagnosticar y tratar la presencia de una fístula cutánea. Caso clínico: Un paciente de sexo masculino, de 9 años de edad, consultó por una lesión cutánea en la zona mandibular del lado izquierdo.
Santiago Frajlich
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