Results 51 to 60 of about 1,069,656 (317)
Multiple familial trichoepitheliomas presenting as leonine facies
Indian Dermatology Online Journal, 2017 Trichoepithelioma is a benign tumor of follicular unit. It has been rarely described as the cause of leonine facies. We are presenting a classical case of multiple familial trichoepitheliomas (MFTs) with characteristic histopathological features leading ...
Sanjay Singh +3 more
doaj +1 more source
Vécu quotidien des personnes de troisième âge dans leur environnement familial et communautaire
Revue des Sciences de la Santé, 2023 L’objectif général de cette étude est de comprendre le vécu des personnes de troisième âge dans leur environnement familial et communautaire dans le quartier MANGENGENGE dans la commune de N’sele.
Benjamin TSHIABA KABITANGAGA +7 more
doaj +1 more source
Pediatric Blood &Cancer, EarlyView.ABSTRACT Purpose Retinoblastoma (RB) is the most common pediatric ocular cancer, yet population‐based data on survival and risk factors remain limited. This study aimed to describe survival in a large national RB cohort and identify predictors of death and complications.
Samuel Sassine +14 more
wiley +1 more source
Acute myeloid leukemia due to germline CEBPA mutation in a Syrian family
Molecular Genetics & Genomic Medicine, 2022 Background Familial cases of adult acute myeloid leukemia (AML) with germline‐mutated CCAAT/enhancer‐binding protein‐α (CEBPA) gene are a rare entity classified in World Health Organization (WHO) classification 2016.
Abdulsamad Wafa +8 more
doaj +1 more source
Video, memory and identity : my body, my history [PDF]
, 2004 Bibliography: leaves 45-47.This explication is an inquiry into familial images of the past and the relationship of these images to history, memory and the present. Because some of these relationships are problematic, alternative ways of looking at memory
Higgs, Jo
core
Cost effectiveness of cascade testing for familial hypercholesterolaemia, based on data from familial hypercholesterolaemia services in the UK [PDF]
, 2017 Peer reviewedPublisher ...
Cather, Moyra +6 more
core +2 more sources
Pediatric Blood &Cancer, EarlyView.ABSTRACT Objective To evaluate selumetinib exposure using therapeutic drug monitoring (TDM) in pediatric patients with neurofibromatosis type 1 (NF1) and plexiform neurofibromas (PN), assess interpatient pharmacokinetic variability, and explore the relationship between drug exposure, clinical response, and adverse effects.
Janka Kovács +8 more
wiley +1 more source
Rare diseases leading to childhood Glaucoma. epidemiology, pathophysiogenesis, and management [PDF]
, 2015 Noteworthy heterogeneity exists in the rare diseases associated with childhood glaucoma. Primary congenital glaucoma is mostly sporadic; however, 10% to 40% of cases are familial. CYP1B1 gene mutations seem to account for 87% of familial cases and 27% of
Abdolrahimzadeh, Solmaz +5 more
core +3 more sources
Salivary melatonin onset in youth at familial risk for bipolar disorder [PDF]
, 2019 Melatonin secretion and polysomnography (PSG) were compared among a group of healthy adolescents who were at high familial risk for bipolar disorder (HR) and a second group at low familial risk (LR).
Armitage, Roseanne +13 more
core +2 more sources
Pediatric Blood &Cancer, EarlyView.ABSTRACT Background and Aims Wilms tumour (WT) has excellent event‐free and overall survival (OS). However, small differences exist between countries participating in the same international study. This led us to examine variation in adherence to protocol recommendations as a potential contributing factor.
Suzanne Tugnait +23 more
wiley +1 more source