Výsledky vyhledávání - "Monia Troudi"

[Acute polyradiculoneuropathy in children: the Kairouan pediatric department experience. Report of 22 cases]

Autor: Fethi, Amri, Zakia, Habboul, Monia, Troudi, M, Ghribi, Hamdi, Guedhami, Nizar, Khattat

Publikováno v: La Tunisie medicale. 89(8-9)

Guillain-Barre Syndrome (GBS) is an acute polyradidulonevritis which is primitive inflammatory and demyelinisant. It represents the most frequent cause of acute peripheric paralysis of the child.To study the epidemiologic, clinic, electromyographic,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e2c1eb152533e7215382fdba02c4dfb9
https://pubmed.ncbi.nlm.nih.gov/21948680

Zobrazit plný text záznamu

Molecular diagnosis of distal renal tubular acidosis in Tunisian patients: proposed algorithm for Northern Africa populations for the ATP6V1B1, ATP6V0A4 and SCL4A1 genes

Autor: Saber Hamami, F. Amri, Wafa Ben Romdane, Gustavo Pérez de Nanclares, Donia Elhayek, Amel Haj Khelil, Nadia Leban, Mohamed Neji Gueddiche, Slaheddine Chouchane, Samir M'Rabet, Monia Troudi, Jemni Ben Chibani, Gema Ariceta, Luis Castaño, Adnene Mlika

Publikováno v: BMC Medical Genetics
Addi. Archivo Digital para la Docencia y la Investigación
instname

Background Primary distal renal tubular acidosis (dRTA) caused by mutations in the genes that codify for the H + −ATPase pump subunits is a heterogeneous disease with a poor phenotype-genotype correlation. Up to now, large cohorts of dRTA Tunisian

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d9194b5f2301257c31892f0a0305f02
http://europepmc.org/articles/PMC4225572

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání