Aller au contenu principal
Profil bibliographique

I. S. Kleimenova

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

3Publications signalées
0Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Muscle Physiology and DisordersCardiomyopathy and Myosin StudiesLysosomal Storage Disorders ResearchGenetic Neurodegenerative DiseasesLong-Term Effects of COVID-19

Les publications récentes

Accès ouvert 2026 article OpenAlex

Neurological complications associated with COVID-19 in a child

Larisa V. Moshurova, О. А. Черкасова, I. S. Kleimenova

The new coronavirus infection associated with the SARS-CoV-2 virus has become one of the global medical and social problems of the 21st century. The SARS-CoV-2 virus, first discovered in 2019, differs from other Coronaviridae viruses SARS-CoV and MERS-CoV in increased contagiousness and …

ru (code pays fourni par la source)

0 citations Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics)
Accès ouvert 2022 article OpenAlex

Myotonia and myotonic discharges of dystrophic myotonia type 1 at the first decade onset: a literature review and data of the case series

С. В. Курбатов, Vladimir Markovich Kenis, Margarita V. Savina, I. S. Kleimenova et autres

Background. Dystrophic myotonia type 1 (DM1) is the most common muscular dystrophy in patients of any age. Myotonia “delayed relaxation of muscle” is the leading symptom in DM1 and can occur at any time after onset disease. Myotonia symptoms and electrical myotonia …

ru, us (code pays fourni par la source)

0 citations Neuromuscular Diseases
Accès ouvert 2015 article OpenAlex

Болезнь Помпе, инфантильная форма (первый случай диагностики в Воронеже)

Valery P. Fedotov, I. S. Kleimenova, Tatyana V. Fedotova, Д. С. Степанов et autres

Pompe disease (PD), or glycogen storage disease type II, is a rare autosomal recessive lysosomal disease caused by glycogen storage in the myocardium, skeletal muscles, and liver. PD, as an orphan disease with a very low prevalence rate, shows a marked clinical …

ru, us (code pays fourni par la source)

0 citations DOAJ (DOAJ: Directory of Open Access Journals)

BNTIC News n’est pas le producteur de ces données. Les publications sont interrogées à la demande dans Crossref, OpenAIRE, DOAJ, Europe PMC, HAL, DataCite, AfricArXiv, ROR et la Banque mondiale, sans clé d’accès. OpenAlex reste optionnel. Aucun service payant n’est nécessaire et aucune donnée externe n’est enregistrée en base. Consulter les sources et leurs limites.