Mirko Baglivo

Milan, 20126, Italy

Last Updated: 09/26/2026

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Found 24 publications

Evaluation of Mitochondrial Dysfunction and Idebenone Responsiveness in Fibroblasts from Leber's Hereditary Optic Neuropathy (LHON) Subjects.

Evaluation of Mitochondrial Dysfunction and Idebenone Responsiveness in Fibroblasts from Leber's Hereditary Optic Neuropathy (LHON) Subjects.

Journal: International journal of molecular sciences

Published: May 31, 2023

A new family with a case of severe early-onset muscle fatigue and a peculiar maternally inherited painful swelling in chewing muscles associated with homoplasmic m.15992A>T mutation in mitochondrial tRNAPro.

A new family with a case of severe early-onset muscle fatigue and a peculiar maternally inherited painful swelling in chewing muscles associated with homoplasmic m.15992A>T mutation in mitochondrial tRNAPro.

Journal: Neuromuscular disorders : NMD

Published: April 27, 2023

CDH5, a Possible New Candidate Gene for Genetic Testing of Lymphedema.

CDH5, a Possible New Candidate Gene for Genetic Testing of Lymphedema.

Journal: Lymphatic research and biology

Published: December 09, 2021

SVEP1 is important for morphogenesis of lymphatic system: Possible implications in lymphedema.

SVEP1 is important for morphogenesis of lymphatic system: Possible implications in lymphedema.

Journal: Lymphology

Published: September 10, 2021

Rare PECAM1 variants in three families with lymphedema.

Rare PECAM1 variants in three families with lymphedema.

Journal: Lymphology

Published: December 22, 2020

Review of the function of SEMA3A in lymphatic vessel maturation and its potential as a candidate gene for lymphedema: Analysis of three families with rare causative variants.

Review of the function of SEMA3A in lymphatic vessel maturation and its potential as a candidate gene for lymphedema: Analysis of three families with rare causative variants.

Journal: Lymphology

Published: November 15, 2020

Segregation Analysis of Rare NRP1 and NRP2 Variants in Families with Lymphedema.

Segregation Analysis of Rare NRP1 and NRP2 Variants in Families with Lymphedema.

Journal: Genes

Published: October 08, 2020

Italian SARS-CoV-2 patients in intensive care: towards an identikit for subjects at risk?

Italian SARS-CoV-2 patients in intensive care: towards an identikit for subjects at risk?

Journal: European review for medical and pharmacological sciences

Published: October 05, 2020

Possible Role of the RORC Gene in Primary and Secondary Lymphedema: Review of the Literature and Genetic Study of Two Rare Causative Variants.

Possible Role of the RORC Gene in Primary and Secondary Lymphedema: Review of the Literature and Genetic Study of Two Rare Causative Variants.

Journal: Lymphatic research and biology

Published: September 22, 2020

Genetic and physiological autonomic nervous system factors involved in failed back surgery syndrome: A review of the literature and report of nine cases treated with pulsed radiofrequency.

Genetic and physiological autonomic nervous system factors involved in failed back surgery syndrome: A review of the literature and report of nine cases treated with pulsed radiofrequency.

Journal: Acta bio-medica : Atenei Parmensis

Published: August 25, 2020

TIE1 as a Candidate Gene for Lymphatic Malformations with or without Lymphedema.

TIE1 as a Candidate Gene for Lymphatic Malformations with or without Lymphedema.

Journal: International journal of molecular sciences

Published: July 28, 2020

Aldo-Keto Reductase 1C1 (AKR1C1) as the First Mutated Gene in a Family with Nonsyndromic Primary Lipedema.

Aldo-Keto Reductase 1C1 (AKR1C1) as the First Mutated Gene in a Family with Nonsyndromic Primary Lipedema.

Journal: International journal of molecular sciences

Published: July 20, 2020

Showing 1-12 of 24

Last Updated: 09/26/2026