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American Journal of Medical Genetics. Part A
|
September 5, 2020
Alazami syndrome: Phenotypic expansion and clinical resemblance to Smith-Lemli-Opitz syndrome
Simone Gana, Massimo Plumari, Elena Rossi, et al.
American Journal of Medical Genetics. Part A
|
May 27, 2024
LZTFL1, a rare cause of Bardet-Biedl syndrome: A new patient with severe short stature and moderate intellectual disability, more than casual associations?
Simone Gana, Marta Di Biagio, Laura Carraro, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 16, 2004
Deep brain stimulation in myoclonus-dystonia syndrome
Laura Cif, Enza Maria Valente, Simone Hemm, et al.
Talanta
|
March 2, 2010
Development of a membraneless extraction module for the extraction of volatile compounds: application in the chromatographic analysis of vicinal diketones in beer
João Grosso Pacheco, Inês Maria Valente, Luís Moreira Gonçalves, et al.
Annals of Neurology
|
November 26, 2002
Clinical and subclinical dopaminergic dysfunction in PARK6-linked parkinsonism: an 18F-dopa PET study
Naheed L Khan, Enza Maria Valente, Anna Rita Bentivoglio, et al.
Geriatrics & Gerontology International
|
August 7, 2015
Mortality in Brazilian community-dwelling older adults: 7 years of follow up in primary care
Talita Cristina Barbosa Rezende Ferreira, Arlete Maria Valente Coimbra, Glaucia Regina Falsarella, et al.
Journal of Medical Genetics
|
August 6, 2021
<i>ARF1</i> haploinsufficiency causes periventricular nodular heterotopia with variable clinical expressivity
Simone Gana, Antonella Casella, Sara Cociglio, et al.
American Journal of Medical Genetics. Part A
|
October 29, 2021
PUS3-related disorder: Report of a novel patient and delineation of the phenotypic spectrum
Alessandro Borghesi, Massimo Plumari, Elena Rossi, et al.
Journal of Neurochemistry
|
January 27, 2009
Mutant Pink1 induces mitochondrial dysfunction in a neuronal cell model of Parkinson's disease by disturbing calcium flux
Roberta Marongiu, Brian Spencer, Leslie Crews, et al.
Nature Reviews. Disease Primers
|
October 21, 2018
Author Correction: Dystonia
Bettina Balint, Niccolò E Mencacci, Enza Maria Valente, et al.
Page
of 36
Search research articles
Search
Showing results (91-100 of 358) with videos related to
Sort By:
Page
of 36
American Journal of Medical Genetics. Part A
|
September 5, 2020
Alazami syndrome: Phenotypic expansion and clinical resemblance to Smith-Lemli-Opitz syndrome
Simone Gana, Massimo Plumari, Elena Rossi, et al.
American Journal of Medical Genetics. Part A
|
May 27, 2024
LZTFL1, a rare cause of Bardet-Biedl syndrome: A new patient with severe short stature and moderate intellectual disability, more than casual associations?
Simone Gana, Marta Di Biagio, Laura Carraro, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 16, 2004
Deep brain stimulation in myoclonus-dystonia syndrome
Laura Cif, Enza Maria Valente, Simone Hemm, et al.
Talanta
|
March 2, 2010
Development of a membraneless extraction module for the extraction of volatile compounds: application in the chromatographic analysis of vicinal diketones in beer
João Grosso Pacheco, Inês Maria Valente, Luís Moreira Gonçalves, et al.
Annals of Neurology
|
November 26, 2002
Clinical and subclinical dopaminergic dysfunction in PARK6-linked parkinsonism: an 18F-dopa PET study
Naheed L Khan, Enza Maria Valente, Anna Rita Bentivoglio, et al.
Geriatrics & Gerontology International
|
August 7, 2015
Mortality in Brazilian community-dwelling older adults: 7 years of follow up in primary care
Talita Cristina Barbosa Rezende Ferreira, Arlete Maria Valente Coimbra, Glaucia Regina Falsarella, et al.
Journal of Medical Genetics
|
August 6, 2021
<i>ARF1</i> haploinsufficiency causes periventricular nodular heterotopia with variable clinical expressivity
Simone Gana, Antonella Casella, Sara Cociglio, et al.
American Journal of Medical Genetics. Part A
|
October 29, 2021
PUS3-related disorder: Report of a novel patient and delineation of the phenotypic spectrum
Alessandro Borghesi, Massimo Plumari, Elena Rossi, et al.
Journal of Neurochemistry
|
January 27, 2009
Mutant Pink1 induces mitochondrial dysfunction in a neuronal cell model of Parkinson's disease by disturbing calcium flux
Roberta Marongiu, Brian Spencer, Leslie Crews, et al.
Nature Reviews. Disease Primers
|
October 21, 2018
Author Correction: Dystonia
Bettina Balint, Niccolò E Mencacci, Enza Maria Valente, et al.
Page
of 36