Results 31 to 40 of about 1,156,853 (299)

ЛЕКАРСТВА И ПЕЧЕНЬ: НЕИЗМЕННЫЙ ТАНДЕМ. ЧАСТЬ 2

open access: yesАрхивъ внутренней медицины, 2012
The article is devoted to the up-to-date data of the drug-induced liver diseases (DILD) problem and series of the clinical monitoring accomplished by the author.
Е. Ю. Еремина
doaj   +1 more source

БИЛИАРНАЯ ПАТОЛОГИЯ И ЕЕ КЛИНИЧЕСКИЕ «МАСКИ». Часть 1

open access: yesАрхивъ внутренней медицины, 2012
The article gives systematicaly organized literature data and the author’s observations of different biliar tract disorder variants. The focus is on the comorbidity formation mechanisms analysis and the difficulties in differential diagnostics of various
Е. Ю. Еремина
doaj   +1 more source

ЛЕКАРСТВА И ПЕЧЕНЬ: НЕИЗМЕННЫЙ ТАНДЕМ. ЧАСТЬ 1

open access: yesАрхивъ внутренней медицины, 2012
The article is devoted to the up-to-date data of the drug-induced liver diseases (DILD) problem and series of the clinical monitoring accomplished by the author.
Е. Ю. Еремина
doaj   +1 more source

Sharing genetic variants with the NGS pipeline is essential for effective genomic data sharing and reproducibility in health information exchange

open access: yesScientific Reports, 2021
Genetic variants causing underlying pharmacogenetic and disease phenotypes have been used as the basis for clinical decision-making. However, due to the lack of standards for next-generation sequencing (NGS) pipelines, reproducing genetic variants among ...
Jeong Hoon Lee   +2 more
doaj   +1 more source

Headache and epilepsy: prevalence and clinical variants

open access: yesНеврология, нейропсихиатрия, психосоматика, 2023
Headache, which is often present in patients with epilepsy, can occur outside of epileptic seizures as well as have a temporary connection with them – occur immediately before, during or after an attack.
V. V. Osipova   +3 more
doaj   +1 more source

Contribution of MUTYH variants to male breast cancer risk: results from a multicenter study in Italy [PDF]

open access: yes, 2018
Inherited mutations in BRCA1, and, mainly, BRCA2 genes are associated with increased risk of male breast cancer (MBC). Mutations in PALB2 and CHEK2 genes may also increase MBC risk.
Azzollini, Jacopo   +25 more
core   +3 more sources

Panniculitis in modern rheumatology [PDF]

open access: yesТерапевтический архив, 2020
Aim. To study clinical and laboratory features of panniculitis (Pn) in modern rheumatology. Materials and methods. The study included 690 patients with Pn (615 women and 75 men, average age 39.410.26) with the prevailing referral diagnosis of Erythema
O. N. Egorova   +3 more
doaj  

Therapeutic ‘masks’ of hypothyroidism

open access: yesMìžnarodnij Endokrinologìčnij Žurnal, 2018
The article deals with the data on various clinical variants of hypothyroidism course. The authors emphasized that establishing early and reliable diagnosis suggests no limitations in ideas about the typical clinical picture of hypothyroidism described ...
V.S. Vernigorodsky   +6 more
doaj   +1 more source

Analysis of neurodegenerative Mendelian genes in clinically diagnosed Alzheimer disease [PDF]

open access: yes, 2017
Alzheimer disease (AD), Frontotemporal lobar degeneration (FTD), Amyotrophic lateral sclerosis (ALS) and Parkinson disease (PD) have a certain degree of clinical, pathological and molecular overlap.
Alexandra Medvedeva   +17 more
core   +4 more sources

Neurosyphilis and Clinical Variants

open access: yesRevista Neurociências, 2012
Introduction. Neurosyphilis is an uncommon manifestation of cen­tral nervous system (CNS) infection caused by Treponema pallidum. Cases. We report three cases of neurosyphilis. Case 1 presented with ocular involvement: right optic atrophy and left optic neuritis; case 2 had a meningovascular form, with ischemic stroke; and case 3, a meningeal form ...
Adriana Moro   +7 more
openaire   +1 more source

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