Lista de obras - M Bertamino - Dominio Público Uruguay

A new form of IRIDA due to combined heterozygous mutations of TMPRSS6 and ACVR1A encoding the BMP receptor ALK2.

artículo científico publicado en 2017

A new short and simple health-related quality of life measurement for paediatric rheumatic diseases: initial validation in juvenile idiopathic arthritis.

artículo científico publicado en 2010

A practical approach to the use of low molecular weight heparins in VTE treatment and prophylaxis in children and newborns

artículo científico publicado en 2014

A prediction rule for lack of achievement of inactive disease with methotrexate as the sole disease-modifying antirheumatic therapy in juvenile idiopathic arthritis

scientific article published on 25 July 2019

Development and initial validation of a radiographic scoring system for the hip in juvenile idiopathic arthritis.

artículo científico publicado en 2009

Diagnosis and management of severe congenital factor XIII deficiency in the Emergency Department: lessons from a "model" family

artículo científico publicado en 2014

Evaluation of 21-numbered circle and 10-centimeter horizontal line visual analog scales for physician and parent subjective ratings in juvenile idiopathic arthritis

artículo científico publicado en 2010

Improved trunk and neck control after selective dorsal rhizotomy in children with spastic cerebral palsy

artículo científico publicado en 2020

International physician survey on management of FOP: a modified Delphi study.

artículo científico publicado en 2017

Long term substrate reduction therapy with ezetimibe alone or associated with statins in three adult patients with lysosomal acid lipase deficiency

artículo científico publicado en 2018

New insights into central nervous system involvement in FOP: Case report and review of the literature.

artículo científico publicado en 2015

Novel asymptomatic CNS findings in patients with ACVR1/ALK2 mutations causing fibrodysplasia ossificans progressiva.

artículo científico publicado en 2016

Novel spondyloepimetaphyseal dysplasia due to UFSP2 gene mutation.

artículo científico publicado en 2017

Outcome and predicting factors of single and multiple intra-articular corticosteroid injections in children with juvenile idiopathic arthritis.

artículo científico publicado en 2011

Perinatal Arterial Ischemic Stroke in Fetal Vascular Malperfusion: A Case Series and Literature Review

scientific article published on 29 October 2020

Widening the Heterogeneity of Leigh Syndrome: Clinical, Biochemical, and Neuroradiologic Features in a Patient Harboring a NDUFA10 Mutation.

artículo científico publicado en 2017

Lista de obras de M Bertamino

A new form of IRIDA due to combined heterozygous mutations of TMPRSS6 and ACVR1A encoding the BMP receptor ALK2.

A new short and simple health-related quality of life measurement for paediatric rheumatic diseases: initial validation in juvenile idiopathic arthritis.

A practical approach to the use of low molecular weight heparins in VTE treatment and prophylaxis in children and newborns

A prediction rule for lack of achievement of inactive disease with methotrexate as the sole disease-modifying antirheumatic therapy in juvenile idiopathic arthritis

Development and initial validation of a radiographic scoring system for the hip in juvenile idiopathic arthritis.

Diagnosis and management of severe congenital factor XIII deficiency in the Emergency Department: lessons from a "model" family

Evaluation of 21-numbered circle and 10-centimeter horizontal line visual analog scales for physician and parent subjective ratings in juvenile idiopathic arthritis

Improved trunk and neck control after selective dorsal rhizotomy in children with spastic cerebral palsy

International physician survey on management of FOP: a modified Delphi study.

Long term substrate reduction therapy with ezetimibe alone or associated with statins in three adult patients with lysosomal acid lipase deficiency

New insights into central nervous system involvement in FOP: Case report and review of the literature.

Novel asymptomatic CNS findings in patients with ACVR1/ALK2 mutations causing fibrodysplasia ossificans progressiva.

Novel spondyloepimetaphyseal dysplasia due to UFSP2 gene mutation.

Outcome and predicting factors of single and multiple intra-articular corticosteroid injections in children with juvenile idiopathic arthritis.

Perinatal Arterial Ischemic Stroke in Fetal Vascular Malperfusion: A Case Series and Literature Review

Widening the Heterogeneity of Leigh Syndrome: Clinical, Biochemical, and Neuroradiologic Features in a Patient Harboring a NDUFA10 Mutation.