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Publications by Roberta Marozzo

A New Family With Transportinopathy: Increased Clinical Heterogeneity

Therapeutic Advances in Neurological Disorders

English

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Heterogeneity in Sepsis: New Biological Evidence With Clinical Applications

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Clinical Heterogeneity Among a Three-Generation Japanese Family With D18N TREX1 Mutation for Aicardi-Goutières Syndrome / Familial Chilblain Lupus

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A Family With a New Elastin Gene Mutation: Broad Clinical Spectrum, Including Sudden Cardiac Death

Cardiology in the Young

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Holidays Apart From Family: Coping With Increased Stress

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Phenotypic Heterogeneity in a Family With FAP Due to a TTR Leu58Arg Mutation: A Clinicopathologic Study

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Clinical Heterogeneity in Fabry Disease

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A New Family With a Homozygous Nonsense Variant in NTHL1 Further Delineated the Clinical Phenotype of NTHL1-associated Polyposis

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Subclinical Nonautoimmune Hyperthyroidism in a Family Segregates With a Thyrotropin Receptor Mutation With Weakly Increased Constitutive Activity

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A New Family of Conjugate Gradient Coefficient With Application

International Journal of Engineering and Technology(UAE)

Chemical Engineering

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Computer Science

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