Results 121 to 130 of about 3,113,716 (239)
Rights and liabilities for people with service animals
Title from web page (viewed Nov. 24, 2004).; "Reviewed in 2003."; Harvested from the web on 11/24/04Ohio Legal Rights Service (OLRS) publication, Rights and Liabilities for People with Service ...
Ohio Legal Rights Service.
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Abstract Objectives Hypertransaminasemia is a frequent finding in hospitalized children with common pediatric illnesses, often considered a transitory phenomenon associated with systemic inflammation/injury. This study aims to assess the prevalence and causes of incidentally detected hypertransaminasemia in children admitted to general pediatric units ...
Angelo Di Giorgio +21 more
wiley +1 more source
Unveiling patriarchy: a systematic review of economic violence against women. [PDF]
Hani SB, Obeisat SA, Hweidi LI.
europepmc +1 more source
Rights and the complaint process for people receiving mental health services
Title from web page (viewed Nov. 29, 2004).; "Reviewed in 2003."; Harvested from the web on 11/30/04Ohio Legal Rights Service (OLRS) publication, Rights and the Complaint Process for People Receiving Mental Health ...
Ohio Legal Rights Service.
core
Abstract Objectives Shwachman–Diamond syndrome (SDS) is an inherited bone marrow failure disorder, and its endoscopic phenotype is poorly defined. We sought to characterize endoscopic findings in patients with genetically confirmed SDS. Methods Retrospective registry study of 45 patients with biallelic Shwachman–Bodian–Diamond syndrome mutations and ...
Elizabeth Korn +15 more
wiley +1 more source
Epistemicide and colonial knowledge: a contrapuntal reading of Nair historiography in South India. [PDF]
Anandhu S, Anupama Nayar CV, Aneesh AS.
europepmc +1 more source
A case report of non‐syndromic colonic ganglioneuroma in a patient with juvenile polyposis
Abstract Colonic ganglioneuromas in children are rare, particularly without associated hereditary syndromes like multiple endocrine neoplasia (MEN2B), neurofibromatosis type 1(NF1), or Phosphatase and tensin homolog hamartoma tumor syndrome (PHTS). We report a 12‐year‐old male with a history of juvenile polyposis syndrome (JPS) and segmental colonic ...
Holly Coffey +2 more
wiley +1 more source
Generalized Nevus Lipomatosus Cutaneous Superficialis: A Case Report with Comprehensive Genetic Analysis. [PDF]
Qiu Y +6 more
europepmc +1 more source
SLC7A6OS Founder Mutation: A Rare Cause of Progressive Myoclonus Epilepsy Dated to 1100 Years Ago
Abstract Background SLC7A6OS c.191A>G is a rare, autosomal recessive cause of progressive myoclonus epilepsy (PME). The c.191A>G variant, first discovered in two families from Türkiye and Portugal, was recently identified in three additional probands from the USA, all of Puerto Rican ancestry.
Bronwyn E. Grinton +17 more
wiley +1 more source
Opportunities to cultivate trust through communication behaviors. [PDF]
Barks MC +7 more
europepmc +1 more source

