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P Da Pozzo

Showing results (11-20 of 15) with videos related to

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Clinical Genetics|July 13, 2011
High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, ItalyG N Gallus, E Cardaioli, A Rufa, et al.
Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica|February 1, 1995
[Role of intraprostatic stents in benign prostatic hypertrophy]V De Luca, G Pezzotti, A Giongo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 17, 2002
Genetic leukoencephalopathies with unknown metabolic pathogenesisA Federico, A Rufa, C Battisti, et al.
Journal of the Neurological Sciences|July 8, 2008
Chronic progressive external ophthalmoplegia: a new heteroplasmic tRNA(Leu(CUN)) mutation of mitochondrial DNAE Cardaioli, P Da Pozzo, E Malfatti, et al.
Journal of the Neurological Sciences|November 8, 2017
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian familiesE Pretegiani, F Rosini, A Rufa, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Clinical Genetics|July 13, 2011
High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, ItalyG N Gallus, E Cardaioli, A Rufa, et al.
Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica|February 1, 1995
[Role of intraprostatic stents in benign prostatic hypertrophy]V De Luca, G Pezzotti, A Giongo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 17, 2002
Genetic leukoencephalopathies with unknown metabolic pathogenesisA Federico, A Rufa, C Battisti, et al.
Journal of the Neurological Sciences|July 8, 2008
Chronic progressive external ophthalmoplegia: a new heteroplasmic tRNA(Leu(CUN)) mutation of mitochondrial DNAE Cardaioli, P Da Pozzo, E Malfatti, et al.
Journal of the Neurological Sciences|November 8, 2017
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian familiesE Pretegiani, F Rosini, A Rufa, et al.
Pageof 2