Lista de obras - Slimane Allali - Dominio Público Uruguay

Accidental mercury poisoning in a 12-year-old girl

artículo científico publicado en 2016

Childhood immune thrombocytopenia: A nationwide cohort study on condition management and outcomes

artículo científico publicado en 2016

Clinical, biological and genetic analysis of anorchia in 26 boys

artículo científico publicado en 2011

Conjugate Haemophilus influenzae type b vaccines for sickle cell disease

artículo científico publicado en 2016

Dramatic improvement after Tocilizumab of a severe COVID-19 in a child with sickle cell disease and acute chest syndrome

scientific article published on 01 May 2020

Efficacy of colchicine in a child with relapsing bullous Henoch-Schönlein purpura.

artículo científico publicado en 2015

Erythrocytic vacuoles that accumulate a fluorescent dye predict spleen size and function in sickle cell disease

artículo científico publicado en 2022

Hepatobiliary Complications in Children with Sickle Cell Disease: A Retrospective Review of Medical Records from 616 Patients

artículo científico publicado en 2019

Innate-like T cells in children with sickle cell disease

artículo científico publicado en 2019

Molecular screening of ADAMTSL2 gene in 33 patients reveals the genetic heterogeneity of geleophysic dysplasia

artículo científico publicado en 2011

Mutation analysis of NR5A1 encoding steroidogenic factor 1 in 77 patients with 46, XY disorders of sex development (DSD) including hypospadias

artículo científico publicado en 2011

Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias

artículo científico publicado en 2011

Plasma histamine elevation in a large cohort of sickle cell disease patients

scientific article published on 28 March 2019

Predicting the adult height of girls with central precocious puberty.

artículo científico publicado en 2011

Presentation of 493 consecutive girls with idiopathic central precocious puberty: a single-center study

artículo científico publicado en 2013

Prevalence and risk factors for red blood cell alloimmunization in 175 children with sickle cell disease in a French university hospital reference centre

artículo científico publicado en 2017

Severe nocturnal and postexercise hypoxia in children and adolescents with sickle cell disease

artículo científico publicado en 2014

Lista de obras de Slimane Allali

Accidental mercury poisoning in a 12-year-old girl

Childhood immune thrombocytopenia: A nationwide cohort study on condition management and outcomes

Clinical, biological and genetic analysis of anorchia in 26 boys

Conjugate Haemophilus influenzae type b vaccines for sickle cell disease

Dramatic improvement after Tocilizumab of a severe COVID-19 in a child with sickle cell disease and acute chest syndrome

Efficacy of colchicine in a child with relapsing bullous Henoch-Schönlein purpura.

Erythrocytic vacuoles that accumulate a fluorescent dye predict spleen size and function in sickle cell disease

Hepatobiliary Complications in Children with Sickle Cell Disease: A Retrospective Review of Medical Records from 616 Patients

Innate-like T cells in children with sickle cell disease

Molecular screening of ADAMTSL2 gene in 33 patients reveals the genetic heterogeneity of geleophysic dysplasia

Mutation analysis of NR5A1 encoding steroidogenic factor 1 in 77 patients with 46, XY disorders of sex development (DSD) including hypospadias

Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias

Plasma histamine elevation in a large cohort of sickle cell disease patients

Predicting the adult height of girls with central precocious puberty.

Presentation of 493 consecutive girls with idiopathic central precocious puberty: a single-center study

Prevalence and risk factors for red blood cell alloimmunization in 175 children with sickle cell disease in a French university hospital reference centre

Severe nocturnal and postexercise hypoxia in children and adolescents with sickle cell disease