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A new case of autosomal dominant small vessel disease carrying a novel heterozygous mutation in HTRA1 gene: 2-year follow-up

Neurological sciences, 2018-08, Vol.39 (8), p.1479-1481

2018

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AARS2-related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases

Acta neurologica Scandinavica, 2018-10, Vol.138 (4), p.278-283

2018

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AARS2‐related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases

Acta neurologica Scandinavica, 2018-10, Vol.138 (4), p.278-283

2018

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Blood–brain barrier permeability in a patient with Labrune syndrome due to SNORD118 mutations

European journal of neurology, 2018-08, Vol.25 (8), p.e86-e87

2018

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Three new mutations in CSF1R gene in 3 Italian patients with hereditary diffuse leukoencephalopathy with axonal spheroids

Journal of the neurological sciences, 2013-10, Vol.333, p.e691-e691

2013

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Two new heterozygous mutations of Htra1 gene in a Caucasian patient affected by CARASIL

Journal of the neurological sciences, 2013-10, Vol.333, p.e660-e660

2013

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DNAJC6 Mutations Associated With Early-Onset Parkinson's Disease

Annals of neurology, 2016-02, Vol.79 (2), p.244-256

2016

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Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism

Human mutation, 2013-09, Vol.34 (9), p.1208-1215

2013

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Idebenone reduces respiratory complications in patients with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2016-08, Vol.26 (8), p.473-480

2016

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Characterization of pulmonary function in 10–18 year old patients with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2017-04, Vol.27 (4), p.307-314

2017

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Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases

Orphanet journal of rare diseases, 2013-08, Vol.8 (1), p.129-129

2013

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The Italian Madrigal: Volume III

1, 2019

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A new case of autosomal dominant small vessel disease carrying a novel heterozygous mutation in HTRA1 gene: 2-year follow-up

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2018, Vol.39 (8), p.1479-1481

2018

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Intellectuals and Reform in the Ottoman Empire: The Young Turks on the challenges of modernity

Taglia, Stefano

1, 2015

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Pragmatism and expediency: Ottoman calculations and the establishment of the Transcaucasian Democratic Federative Republic

Caucasus survey, 2020-01, Vol.8 (1), p.45-58

Taglia, Stefano

2020

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Ottomanism Then and Now: Historical and Contemporary Meanings

Welt des Islams, 2016 (3-4), p.279-289

Taglia, Stefano

2016

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Ottomanism Then and Now: Historical and Contemporary Meanings: An Introduction

Welt des Islams, 2016-01, Vol.56 (3/4), p.279-289

Taglia, Stefano

2016

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The Feasibility of Ottomanism as a Nationalist Project: The View of Albanian Young Turk İsmail Kemal

Welt des Islams, 2016-01, Vol.56 (3-4), p.336-358

Taglia, Stefano

2016

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Drug‐induced psoriasiform alopecia associated with interleukin‐17 inhibitor therapy

Journal of cutaneous pathology, 2021-06, Vol.48 (6), p.771-774

2021

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Becoming Ottomans: Sephardi Jews and Imperial Citizenship in the Modern Era, by Julia Phillips Cohen

The English historical review, 2015-12, Vol.130 (547), p.1579-1580

Taglia, Stefano

2015

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Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy

PloS one, 2015-10, Vol.10 (10), p.e0141240-e0141240

2015

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Malek Sharif. Imperial Norms and Local Realities – The Ottoman Municipal Laws and the Municipality of Beirut (1860–1908)

Archiv orientální, 2015-05, Vol.83 (1), p.207-212

Taglia, Stefano

2015

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Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): update on molecular genetics

Neurological sciences, 2016-09, Vol.37 (9), p.1565-1569

2016

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Fibroblast growth factor 21 and grow differentiation factor 15 are sensitive biomarkers of mitochondrial diseases due to mitochondrial transfer-RNA mutations and mitochondrial DNA deletions

Neurological sciences, 2020-12, Vol.41 (12), p.3653-3662

2020

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Primary familial brain calcification: update on molecular genetics

Neurological sciences, 2015-05, Vol.36 (5), p.787-794

2015

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A new case of autosomal dominant small vessel disease carrying a novel heterozygous mutation in HTRA1 gene: 2-year follow-up

AARS2-related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases

AARS2‐related ovarioleukodystrophy: Clinical and neuroimaging features of three new cases

Blood–brain barrier permeability in a patient with Labrune syndrome due to SNORD118 mutations

Three new mutations in CSF1R gene in 3 Italian patients with hereditary diffuse leukoencephalopathy with axonal spheroids

Two new heterozygous mutations of Htra1 gene in a Caucasian patient affected by CARASIL

DNAJC6 Mutations Associated With Early-Onset Parkinson's Disease

Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism

Idebenone reduces respiratory complications in patients with Duchenne muscular dystrophy

Characterization of pulmonary function in 10–18 year old patients with Duchenne muscular dystrophy

Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases

The Italian Madrigal: Volume III

A new case of autosomal dominant small vessel disease carrying a novel heterozygous mutation in HTRA1 gene: 2-year follow-up

Intellectuals and Reform in the Ottoman Empire: The Young Turks on the challenges of modernity

Pragmatism and expediency: Ottoman calculations and the establishment of the Transcaucasian Democratic Federative Republic

Ottomanism Then and Now: Historical and Contemporary Meanings

Ottomanism Then and Now: Historical and Contemporary Meanings: An Introduction

The Feasibility of Ottomanism as a Nationalist Project: The View of Albanian Young Turk İsmail Kemal

Drug‐induced psoriasiform alopecia associated with interleukin‐17 inhibitor therapy

Becoming Ottomans: Sephardi Jews and Imperial Citizenship in the Modern Era, by Julia Phillips Cohen

Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy

Malek Sharif. Imperial Norms and Local Realities – The Ottoman Municipal Laws and the Municipality of Beirut (1860–1908)

Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): update on molecular genetics

Fibroblast growth factor 21 and grow differentiation factor 15 are sensitive biomarkers of mitochondrial diseases due to mitochondrial transfer-RNA mutations and mitochondrial DNA deletions

Primary familial brain calcification: update on molecular genetics

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