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Clinical phenotypes in sarcoidosis
(Lippincott Williams & Wilkins, 2014-09-01)
Purpose of reviewTo describe the methods for derivation of clinical phenotypes in general and how they should be applied in sarcoidosis, taking into account the dimensions of the disease. the results from the small number ...
Phenotypic characteristics associated with virulence of clinical isolates from the Sporothrix complex
(Hindawi Publishing Corporation, 2019)
Temporal Design Patterns for Digital Phenotype Cohort Selection in Critical Care:Systematic Literature Assessment and Qualitative Synthesis
(2020)
Background: Inclusion criteria for observational studies frequently contain temporal entities and relations. The use of digital phenotypes to create cohorts in electronic health record–based observational studies requires ...
For which infants with viral bronchiolitis could it be deemed appropriate to use albuterol, at least on a therapeutic trial basis?
(2021)
Although there is increasing evidence showing that infants with viral bronchiolitis exhibit a high degree of heterogeneity, a core uncertainty shared by many clinicians is with regard to understanding which patients are ...
An Up-to-Date Overview of the Complexity of Genotype-Phenotype Relationships in Myotonic Channelopathies
(2020-01)
Myotonic disorders are inherited neuromuscular diseases divided into dystrophic myotonias and non-dystrophic myotonias (NDM). The latter is a group of dominant or recessive diseases caused by mutations in genes encoding ...
A systematic review of treatment of Painful Diabetic Neuropathy by Pain Phenotype versus treatment Based on Medical comorbidities
(Frontiers Media Sa, 2017)
Background: Painful diabetic neuropathy (PDN) is a serious, polymorphic, and prevalent complication of diabetes mellitus. Most PDN treatment guidelines recommend a selection of drugs based on patient comorbidities. Despite ...
New Approach To Phenotypic Variability And Karyotype-phenotype Correlation In Turner Syndrome
(WALTER DE GRUYTER GMBHBERLIN, 2016)
New Approach To Phenotypic Variability And Karyotype-phenotype Correlation In Turner Syndrome
(Walter de Gruyter GMBHBerlin, 2016)