Suchergebnisse - "Vazza, Giovanni"

PubPharm (45)

1

The Methylation Analysis of the Glucose-Dependent Insulinotropic Polypeptide Receptor (GIPR) Locus in GH-Secreting Pituitary Adenomas

enthalten in: International journal of molecular sciences | 2023

von Dalle Nogare, M. | D'Annunzio, S. | Vazza, G. | +7

2

Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia

enthalten in: Brain : a journal of neurology | 2022

von Méreaux, J. | Banneau, G. | Papin, M. | +34

3

Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4 : A Cross-sectional Study by the Italian DAISY Network

enthalten in: Neurology. Genetics | 2022

von Rossi, S. | Rubegni, A. | Riso, V. | +46

4

Internal validation and improvement of mitochondrial genome sequencing using the Precision ID mtDNA Whole Genome Panel

enthalten in: International journal of legal medicine | 2021

von Faccinetto, C. | Sabbatini, D. | Serventi, P. | +10

5

Correction : Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2021

von Roux, T. | Barbier, M. | Papin, M. | +93

ErratumFor: Genet Med. 2020 Nov;22(11):1851-1862. - PMID 32713943

6

Internal validation and improvement of mitochondrial genome sequencing using the Precision ID mtDNA Whole Genome Panel

enthalten in: International journal of legal medicine | 2021

von Faccinetto, C. | Sabbatini, D. | Serventi, P. | +10

7

Internal validation and improvement of mitochondrial genome sequencing using the Precision ID mtDNA Whole Genome Panel

enthalten in: International journal of legal medicine | 2021

von Faccinetto, C. | Sabbatini, D. | Serventi, P. | +10

8

Internal validation and improvement of mitochondrial genome sequencing using the Precision ID mtDNA Whole Genome Panel

enthalten in: International journal of legal medicine | 2021

von Faccinetto, C. | Sabbatini, D. | Serventi, P. | +10

9

Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlations

enthalten in: Neurogenetics | 2021

von Méreaux, J. | Firanescu, C. | Coarelli, G. | +26

10

Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlations

enthalten in: Neurogenetics | 2021

von Méreaux, J. | Firanescu, C. | Coarelli, G. | +26

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