Results 81 to 90 of about 436,550 (248)

Chronic nausea and vomiting syndrome and impact on quality of life

open access: yesRevista de Gastroenterología de México (English Edition)
Introduction and aim: Chronic nausea and vomiting syndrome is a disorder of gut-brain interaction that affects the productive-age population. Our aim was to determine the association of this disorder with quality of life, workplace performance, and ...
F.A. Félix-Téllez   +6 more
doaj   +1 more source

Gastrointestinal Manifestations in Rubinstein‐Taybi Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Rubinstein–Taybi syndrome is a rare genetic condition associated with a wide range of physical, cognitive, and developmental impairments, yet its gastrointestinal manifestations remain poorly characterized. Case reports and small series suggest a high prevalence of gastroesophageal reflux, constipation, dysphagia, and nutritional compromise ...
Mohamad Abi Nassif   +3 more
wiley   +1 more source

Nausea in Specific Phobia of Vomiting

open access: yesBehavioral Sciences, 2013
Specific phobia of vomiting (SPOV) is a clinical condition with early onset, chronic course and substantial psychosocial impairment due to a rigorous avoidance behavior. A primary symptom which drives patients to consult a medical practitioner is nausea.
Eugen Trinka   +3 more
doaj   +1 more source

Angelus and other false demons: Sacred counterwriting in Blanca Varela’s poetry [PDF]

open access: yes, 2019
En este trabajo se analizará el proceso de reescritura y desmitificación al que Blanca Varela somete el texto bíblico. A través de la profanización de diversas figuras del canon católico y especialmente del diálogo truncado con un Dios ausente, Varela ...
Velayos Amo, Beatriz
core   +2 more sources

The 9th International RASopathies Symposium

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The RASopathies are a group of congenital disorders with overlapping clinical manifestations that are caused by pathogenic germline or early somatic variants that result in the hyperactivation of the RAS/mitogen‐activated protein kinase (MAPK) signaling pathway.
Pau Castel   +41 more
wiley   +1 more source

Utilização de antieméticos no tratamento antineoplásico de pacientes oncológicos

open access: yesRevista Brasileira de Farmácia Hospitalar e Serviços de Saúde, 2019
Os medicamentos antineoplásicos exercem sua função contra o câncer trazendo inúmeros efeitos colaterais ao paciente. Para os esquemas de tratamento usualmente empregados, os efeitos colaterais mais freqüentes são náuseas e vômitos.
JULIANA BECKER, JEANINE MARIE NARDIN
doaj  

Acquired food aversion and quality of life in women with beast cancer [PDF]

open access: yes, 2009
OBJETIVO: Avaliar o comportamento alimentar de mulheres com câncer de mama submetidas à quimioterapia, e sua relação com a qualidade de vida destas pacientes.
DAMASCENO, Nágila Raquel Teixeira   +3 more
core   +2 more sources

Targeted Anti‐IL‐1 Immunomodulatory Therapy in Pediatric Onset PPP1R13L‐Related Arrhythmogenic Cardiomyopathy

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Autosomal recessive loss‐of‐function variants in PPP1R13L cause an ultra‐rare cardiocutaneous syndrome characterized by rapidly progressive arrhythmogenic cardiomyopathy (ACM). PPP1R13L encodes iASPP, which has two potentially overlapping mechanisms driving ACM as both a regulator of NFκB‐mediated inflammation and a binding partner within the ...
Aaron Renberg   +9 more
wiley   +1 more source

Jean-Paul Sartre : el filósofo necesario [PDF]

open access: yes, 2005
"Leer a Sartre es una necesidad para todo aficionado a la filosofía, si concibe a esta práctica como un\nejercicio del pensamiento que traza líneas de fuga en los saberes establecidos." Estas palabras de\nTomás Abraham seguro han de ser las más indicadas
Abraham, Tomás
core  

Diagnostic Odyssey of Atypical Long‐Chain 3‐Hydroxyacyl‐CoA Dehydrogenase Deficiency (LCHADD) Explained by Three Allelic Products From Two Pathogenic Variants

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency (LCHADD) is an autosomal recessive mitochondrial defect of long‐chain fatty acid β‐oxidation, caused by biallelic pathogenic variants in HADHA or HADHB. We report a 22‐year‐old male with an atypically mild presentation of LCHADD who was referred to the Undiagnosed Diseases Network (UDN ...
Yutaka Furuta   +9 more
wiley   +1 more source

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