Politano, Luisa: search on Z-Library

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1

Syrian hamster infected with Leishmania infantum: A new experimental model for inflammatory myopathies

Orlando Paciello, Slawomir Wojcik, Luigi Gradoni, Gaetano Oliva, Francesca Trapani, Valentina Iovane, Luisa Politano, Serenella Papparella

Journal:

Year:

2010

Language:

english

File:

PDF, 377 KB

english, 2010

2

Determining the role of skewed X-chromosome inactivation in developing muscle symptoms in carriers of Duchenne muscular dystrophy

Viggiano, Emanuela, Ergoli, Manuela, Picillo, Esther, Politano, Luisa

Journal:

Year:

2016

Language:

english

File:

PDF, 596 KB

english, 2016

3

The variability of SMCHD1 gene in FSHD patients: evidence of new mutations

Strafella, Claudia, Caputo, Valerio, Galota, Rosaria Maria, Campoli, Giulia, Bax, Cristina, Colantoni, Luca, Minozzi, Giulietta, Orsini, Chiara, Politano, Luisa, Tasca, Giorgio, Novelli, Giuseppe, Ric

Journal:

Human Molecular Genetics

Year:

2019

Language:

english

File:

PDF, 804 KB

english, 2019

4

Evaluation of the cardiomyopathy in becker muscular dystrophy

Dr. Giovanni Nigro, Lucia I. Comi, Luisa Politano, Francesco M. Limongelli, Vincenzo Nigro, Maria L. De Rimini, Maria A. M. Giugliano, Vito R. Petretta, Luigia Passamano, Brunella Restucci, Luciano Fa

Journal:

Year:

1995

Language:

english

File:

PDF, 2.39 MB

english, 1995

5

Prospective study of X-linked progressive muscular dystrophy in campania

Professor Giovanni Nigro, Lucia I. Comi, Francesco M. Limongelli, Maria Antonietta M. Giugliano, Luisa Politano, Vito Petretta, Luigia Passamano, Severo Stefanelli

Journal:

Year:

1983

Language:

english

File:

PDF, 672 KB

english, 1983

6

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

Filocamo, Mirella, Baldo, Chiara, Goldwurm, Stefano, Renieri, Alessandra, Angelini, Corrado, Moggio, Maurizio, Mora, Marina, Merla, Giuseppe, Politano, Luisa, Garavaglia, Barbara, Casareto, Lorena, Br

Journal:

Orphanet Journal of Rare Diseases

Year:

2013

Language:

english

File:

PDF, 1.25 MB

english, 2013

7

Dilated Cardiomyopathy of Muscular Dystrophy: A Multifaceted Approach to Management

Nigro, Giovanni, Comi, Lucia, Politano, Luisa, Nigro, Vincenzo

Journal:

Seminars in Neurology

Year:

1995

Language:

english

File:

PDF, 364 KB

english, 1995

8

The analysis of myotonia congenita mutations discloses functional clusters of amino acids within CBS2 domain and C-terminal peptide of ClC-1 channel

Altamura, Concetta, Lucchiari, Sabrina, Sahbani, Dalila, Ulzi, Gianna, Comi, Giacomo P., D'Ambrosio, Paola, Petillo, Roberta, Politano, Luisa, Vercelli, Liliana, Mongini, Tiziana, Dotti, Maria Teresa,

Journal:

Year:

2018

Language:

english

File:

PDF, 2.15 MB

english, 2018

9

Pulsed doppler tissue imaging in dystrophinopathic cardiomyopathy

Agretto, Angelo, Politano, Luisa, Bossone, Eduardo, Petretta, Vito R., D'Isa, Salvatore, Passamano, Luigia, Comi, Lucia I., Erbel, Raimund

Journal:

Journal of the American Society of Echocardiography

Year:

2002

Language:

english

File:

PDF, 585 KB

english, 2002

10

Cross-sectional serum metabolomic study of multiple forms of muscular dystrophy

Spitali, Pietro, Hettne, Kristina, Tsonaka, Roula, Sabir, Ekrem, Seyer, Alexandre, Hemerik, Jesse B.A., Goeman, Jelle J., Picillo, Esther, Ergoli, Manuela, Politano, Luisa, Aartsma-Rus, Annemieke

Journal:

Journal of Cellular and Molecular Medicine

Year:

2018

Language:

english

File:

PDF, 424 KB

english, 2018

11

Prevalence of Left Ventricular Systolic Dysfunction in Myotonic Dystrophy Type 1: A Systematic Review

Russo, Vincenzo, Sperlongano, Simona, Gallinoro, Emanuele, Rago, Anna, Papa, Andrea Antonio, Golino, Paolo, Politano, Luisa, Nazarian, Saman, Nigro, Gerardo

Journal:

Journal of Cardiac Failure

Year:

2019

Language:

english

File:

PDF, 191 KB

english, 2019

12

Skeletal muscle cytochrome c in X-linked muscle dystrophies

Giovanni Nigro, Lucia I. Comi, Luisa Politano, Francesco M. Limongelli

Journal:

Clinica Chimica Acta

Year:

1991

Language:

english

File:

PDF, 325 KB

english, 1991

13

Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements

D'Amico, Adele, Catteruccia, Michela, Baranello, Giovanni, Politano, Luisa, Govoni, Alessandra, Previtali, Stefano Carlo, Pane, Marika, D'Angelo, Maria Grazia, Bruno, Claudio, Messina, Sonia, Ricci, F

Journal:

Neuromuscular Disorders

Year:

2017

Language:

english

File:

PDF, 679 KB

english, 2017

14

Clarification on Uveal Melanoma Associated With Myotonic Dystrophy

Rosa, Nicola, De Bernardo, Maddalena, Politano, Luisa

Journal:

JAMA Ophthalmology

Year:

2018

Language:

english

File:

PDF, 41 KB

english, 2018

15

P-Wave Duration and Dispersion in Patients With Emery-Dreifuss Muscular Dystrophy

Russo, Vincenzo, Rago, Anna, Palladino, Alberto, Papa, Andrea Antonio, Di Meo, Federica, Della Cioppa, Nadia, Golino, Paolo, Russo, Maria Giovanna, Calabrò, Raffaele, Politano, Luisa, Nigro, Gerardo

Journal:

Journal of Investigative Medicine

Year:

2011

Language:

english

File:

PDF, 109 KB

english, 2011

16

Heart transplantation in patients with dystrophinopathic cardiomyopathy: Review of the literature and personal series

Papa, Andrea Antonio, D'Ambrosio, Paola, Petillo, Roberta, Palladino, Alberto, Politano, Luisa

Journal:

Intractable & Rare Diseases Research

Year:

2017

Language:

english

File:

PDF, 446 KB

english, 2017

17

CLCN1 Molecular Characterization in 19 South-Italian Patients With Dominant and Recessive Type of Myotonia Congenita

Orsini, Chiara, Petillo, Roberta, D'Ambrosio, Paola, Ergoli, Manuela, Picillo, Esther, Scutifero, Marianna, Passamano, Luigia, De Luca, Alessandro, Politano, Luisa

Journal:

Frontiers in Neurology

Year:

2020

File:

PDF, 483 KB

2020

18

Sarcoglycanopathies and the risk of undetected deletion alleles in diagnosis

Stefan J. White, Shirley Uitte de Willige, Dennis Verbove, Luisa Politano, Ieke Ginjaar, Martijn H. Breuning, Johan T. den Dunnen

Journal:

Year:

2005

Language:

english

File:

PDF, 138 KB

english, 2005

19

Role of electrophysiological evaluation for the best device choice to prevent sudden cardiac death in patients with Myotonic Dystrophy Type 1 and Emery Dreifuss Muscular Dystrophy

Russo, Vincenzo, Politano, Luisa, Nigro, Gerardo

Journal:

Trends in Cardiovascular Medicine

Year:

2017

Language:

english

File:

PDF, 708 KB

english, 2017

20

Intraocular Pressure in Patients with Muscular Dystrophies

Rosa, Nicola, Lanza, Michele, de Bernardo, Maddalena, Cecio, Maria Rosaria, Passamano, Luigia, Politano, Luisa

Journal:

Year:

2013

Language:

english

File:

PDF, 163 KB

english, 2013

21

Emerging perspectives on laminopathies

Politano, Luisa, Lattanzi, Giovanna, Benedetti, Sara, D'Apice, Maria Rosaria, Maggi, Lorenzo, Carboni, Nicola, Scarano, Emanuela

Journal:

Cell Health and Cytoskeleton

Year:

2016

File:

PDF, 366 KB

2016

22

Detection of a nonsense mutation in the dystrophin gene by multiple SSCP

Nigro, Vincenzo, Politano, Luisa, Nigro, Giovanni, Romano, Sergio Colonna, Molinari, Anna Maria, Puca, Giovanni Alfredo

Journal:

Human Molecular Genetics

Year:

1992

Language:

english

File:

PDF, 1.48 MB

english, 1992

23

The position of nonsense mutations can predict the phenotype severity: A survey on the DMD gene

Torella, Annalaura, Zanobio, Mariateresa, Zeuli, Roberta, del Vecchio Blanco, Francesca, Savarese, Marco, Giugliano, Teresa, Garofalo, Arcomaria, Piluso, Giulio, Politano, Luisa, Nigro, Vincenzo, Sing

Journal:

Year:

2020

File:

PDF, 1.20 MB

2020

24

Cardiac and Neuromuscular Features of Patients With LMNA -Related Cardiomyopathy

Peretto, Giovanni, Di Resta, Chiara, Perversi, Jacopo, Forleo, Cinzia, Maggi, Lorenzo, Politano, Luisa, Barison, Andrea, Previtali, Stefano C., Carboni, Nicola, Brun, Francesca, Pegoraro, Elena, D'Ami

Journal:

Annals of Internal Medicine

Year:

2019

File:

PDF, 138 KB

2019

25

Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for “double trouble” overlapping syndromes

Giulia Ricci, Isabella Scionti, Greta Alì, Leda Volpi, Virna Zampa, Marina Fanin, Corrado Angelini, Luisa Politano, Rossella Tupler, Gabriele Siciliano

Journal:

Neuromuscular Disorders

Year:

2012

Language:

english

File:

PDF, 727 KB

english, 2012

26

Emerging perspectives on laminopathies

Politano, Luisa, Lattanzi, Giovanna, Benedetti, Sara, D'Apice, Maria Rosaria, Maggi, Lorenzo, Carboni, Nicola, Scarano, Emanuela

Journal:

Cell Health and Cytoskeleton

Year:

2016

Language:

english

File:

PDF, 366 KB

english, 2016

27

Autonomic nervous system imbalance and left ventricular systolic dysfunction as potential candidates for arrhythmogenesis in Becker muscular dystrophy

Valentino Ducceschi, Gerardo Nigro, Berardo Sarubbi, Lucia I Comi, Luisa Politano, Vito R Petretta, Stefano Nardi, Nicola Briglia, Lucio Santangelo, Giovanni Nigro, Aldo Iacono

Journal:

International Journal of Cardiology

Year:

1997

Language:

english

File:

PDF, 77 KB

english, 1997

28

Giovanni Nigro 1931–2017

Politano, Luisa, Nigro, Vincenzo

Journal:

Neuromuscular Disorders

Year:

2018

Language:

english

File:

PDF, 421 KB

english, 2018

29

Early onset of cardiomyopathy and primary prevention of sudden death in X-linked Emery–Dreifuss muscular dystrophy

Gerardo Nigro, Vincenzo Russo, Vega Maria Ventriglia, Nadia Della Cioppa, Alberto Palladino, Vincenzo Nigro, Raffaele Calabrò, Giovanni Nigro, Luisa Politano

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 1.81 MB

english, 2010

30

Novel small mutations along the DMD/BMD gene associated with different phenotypes

Nigro, Vincenzo, Nigro, Giovanni, Esposito, Maria Grazia, Comi, Lucia Ines, Molinari, Anna Maria, Puca, Giovanni Alfredo, Politano, Luisa

Journal:

Human Molecular Genetics

Year:

1994

Language:

english

File:

PDF, 194 KB

english, 1994

31

Mutation of dystrophin gene and cardiomyopathy

Nigro, Giovanni, Politano, Luisa, Nigro, Vincenzo, Petretta, Vito R., Comi, Lucia I.

Journal:

Neuromuscular Disorders

Year:

1994

Language:

english

File:

PDF, 1.65 MB

english, 1994

32

Galactose-1-Phosphate Uridyltransferase deficiency: a literature review of the putative mechanisms of short and long-term complications and allelic variants

Viggiano, Emanuela, Marabotti, Anna, Politano, Luisa, Burlina, Alberto

Journal:

Clinical Genetics

Year:

2017

Language:

english

File:

PDF, 1.22 MB

english, 2017

33

ACE inhibition to slow progression of myocardial fibrosis in muscular dystrophies

Russo, Vincenzo, Papa, Andrea Antonio, Williams, Emmanuel Ato, Rago, Anna, Palladino, Alberto, Politano, Luisa, Nigro, Gerardo

Journal:

Trends in Cardiovascular Medicine

Year:

2017

Language:

english

File:

PDF, 650 KB

english, 2017

34

Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene

Nigro, Vincenzo, Moreira, Eloisa de Sá, Piluso, Giulio, Vainzof, Mariz, Belsito, Angela, Politano, Luisa, Puca, Annibale A., Passos-Bueno, Maria Rita, Zatz, Mayana

Journal:

Nature Genetics

Year:

1996

File:

PDF, 532 KB

1996

35

Intraocular Pressure and Corneal Biomechanical Properties in Patients with Myotonic Dystrophy

Nicola Rosa, Michele Lanza, Maria Borrelli, Alberto Palladino, M. Grazia Di Gregorio, Luisa Politano

Journal:

Year:

2009

Language:

english

File:

PDF, 430 KB

english, 2009

36

Corneal Thickness and Endothelial Cell Characteristics in Patients with Myotonic Dystrophy

Nicola Rosa, Michele Lanza, Maria Borrelli, Maria Luisa Filosa, Maddalena De Bernardo, Vega Maria Ventriglia, Maria Rosaria Cecio, Luisa Politano

Journal:

Year:

2010

Language:

english

File:

PDF, 142 KB

english, 2010

37

Molecular and muscle pathology in a series of caveolinopathy patients

Luigi Fulizio, Anna Chiara Nascimbeni, Marina Fanin, Giulio Piluso, Luisa Politano, Vincenzo Nigro, Corrado Angelini

Journal:

Year:

2005

Language:

english

File:

PDF, 274 KB

english, 2005

38

Prevalence of the 550delA mutation in calpainopathy (LGMD 2A) in Croatia

Nina Canki-Klain, Astrid Milic, Biserka Kovac, Anuska Trlaja, Damir Grgicevic, Niko Zurak, Michel Fardeau, France Leturcq, Jean-Claude Kaplan, J. Andoni Urtizberea, Luisa Politano, Giulio Piluso, Josu

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 104 KB

english, 2004

39

Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutations

Cacciottolo, Mafalda, Numitone, Gelsomina, Aurino, Stefania, Caserta, Imma Rosaria, Fanin, Marina, Politano, Luisa, Minetti, Carlo, Ricci, Enzo, Piluso, Giulio, Angelini, Corrado

Journal:

European Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 541 KB

english, 2011

40

Development of Cardiomyopathy in Female Carriers of Duchenne and Becker Muscular Dystrophies

Politano, Luisa

Journal:

JAMA The Journal of the American Medical Association

Year:

1996

Language:

english

File:

PDF, 3.71 MB

english, 1996

41

Cardiac Function in Types II and III Spinal Muscular Atrophy: Should We Change Standards of Care?

Bianco, Flaviana, Pane, Marika, D'Amico, Adele, Messina, Sonia, Delogu, Angelica, Soraru, Gianni, Pera, Maria, Mongini, Tiziana, Politano, Luisa, Baranello, Giovanni, Vita, Gianluca, Tiziano, Francesc

Journal:

Neuropediatrics

Year:

2014

Language:

english

File:

PDF, 81 KB

english, 2014

42

Anterior capsule phimosis and capsular block syndrome in a patient with Steinert myotonic dystrophy: a case report

Rosa, Nicola, Lanza, Michele, De Bernardo, Maddalena, Borrelli, Maria, Politano, Luisa

Journal:

Year:

2009

Language:

english

File:

PDF, 1.15 MB

english, 2009

43

Cardiac involvement in laminopathies – short invited review

Nigro, Gerardo, Carboni, Nicola, Marchel, Michal, Palladino, Alberto, Madej-Pilarczyk, Agnieszka, Opolski, Grzegorz, Hausmanowa-Petrusewicz, Irena, Politano, Luisa

Journal:

Family Medicine & Primary Care Review

Year:

2015

File:

PDF, 169 KB

2015

44

Study of expression of genes potentially responsible for reduced fitness in patients with myotonic dystrophy type 1 and identification of new biomarkers of testicular function

Ergoli, Manuela, Venditti, Massimo, Picillo, Esther, Minucci, Sergio, Politano, Luisa

Journal:

Molecular Reproduction and Development

Year:

2019

File:

PDF, 988 KB

2019

45

SSCP analysis of the emerin gene

Luisa Politano, Vincenzo Nigro

Journal:

Neuromuscular Disorders

Year:

1996

Language:

english

File:

PDF, 107 KB

english, 1996

46

Low Intraocular Pressure Resulting from Ciliary Body Detachment in Patients with Myotonic Dystrophy

Nicola Rosa, Michele Lanza, Maria Borrelli, Maddalena De Bernardo, Alberto Palladino, Maria Grazia Di Gregorio, Fabrizia Pascotto, Luisa Politano

Journal:

Year:

2011

Language:

english

File:

PDF, 408 KB

english, 2011

47

Giovanni Nigro 1931–2017

Politano, Luisa, Nigro, Vincenzo

Journal:

Neuromuscular Disorders

Year:

2018

File:

PDF, 421 KB

2018

48

Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2H

Valentina Saccone, Michela Palmieri, Luigia Passamano, Giulio Piluso, Germana Meroni, Luisa Politano, Vincenzo Nigro

Journal:

Year:

2008

Language:

english

File:

PDF, 371 KB

english, 2008

49

Muscular dystrophies: key elements for everyday diagnosis and management

Palladino, Alberto, Nigro, Gerardo, Politano, Luisa

Journal:

Year:

2013

Language:

english

File:

PDF, 1010 KB

english, 2013

50

Managing dystrophinopathic cardiomyopathy

Politano, Luisa, Nigro, Giovanni

Journal:

Expert Opinion on Orphan Drugs

Year:

2016

Language:

english

File:

PDF, 2.55 MB

english, 2016

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