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Muglia, M.
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1

Observations of Shelf‐Ocean Exchange in the Northern South ..:

Andres, M. ; Muglia, M. ; Seim, H...
Journal of Geophysical Research: Oceans.  128 (2023)  7 - p. , 2023
Link: https://doi.org/10.1029/..
 
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2

A low-order wake interaction modeling framework for the per..:

Razi, P. ; Ramaprabhu, P. ; Tarey, P...
Renewable Energy.  200 (2022)  - p. 1602-1617 , 2022
Link: https://doi.org/10.1016/..
 
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3

A 71‐nucleotide deletion in the periaxin gene in an Italian..:

Citrigno, L. ; Zoccolella, S. ; Lastella, P...
European Journal of Neurology.  27 (2020)  10 - p. 2109-2110 , 2020
Link: https://doi.org/10.1111/..
 
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4

Kinesins in neurological inherited diseases: a novel motor-..:

Citrigno, L. ; Magariello, A. ; Pugliese, P....
Acta Neurologica Belgica.  118 (2018)  4 - p. 643-646 , 2018
Link: https://doi.org/10.1007/..
 
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5

Exome sequencing reveals twoFA2Hmutations in a family with ..:

Magariello, A. ; Russo, C. ; Citrigno, L....
Journal of the Neurological Sciences.  372 (2017)  - p. 347-349 , 2017
Link: https://doi.org/10.1016/..
 
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6

The role of glucocorticoid receptor-dependent activity in t..:

Arnett, M G ; Pan, M S ; Doak, W...
Translational Psychiatry.  5 (2015)  4 - p. e542-e542 , 2015
Link: https://doi.org/10.1038/..
 
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7

A novel KIF5A mutation in an Italian family marked by spast..:

Muglia, M. ; Citrigno, L. ; D'Errico, E....
Journal of the Neurological Sciences.  343 (2014)  1-2 - p. 218-220 , 2014
Link: https://doi.org/10.1016/..
 
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8

Further evidence that DDHD2 gene mutations cause autosomal ..:

Magariello, A. ; Citrigno, L. ; Zuchner, S....
European Journal of Neurology.  21 (2014)  3 - p. , 2014
Link: https://doi.org/10.1111/..
 
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9

The natural history of spinal neurofibromatosis: a critical..:

Ruggieri, M. ; Polizzi, A. ; Spalice, A....
Clinical Genetics.  87 (2014)  5 - p. 401-410 , 2014
Link: https://doi.org/10.1111/..
 
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10

First mutation in the nuclear localization signal sequence ..:

Magariello, A. ; Tortorella, C. ; Patitucci, A....
European Journal of Neurology.  20 (2012)  1 - p. , 2012
Link: https://doi.org/10.1111/..
 
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11

SEVERE CMT TYPE 2 WITH FATAL ENCEPHALOPATHY ASSOCIATED WITH..:

Boaretto, F. ; Vettori, A. ; Casarin, A....
Neurology.  74 (2010)  23 - p. 1919-1921 , 2010
Link: https://doi.org/10.1212/..
 
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12

CADASIL: Extended polymorphisms and mutational analysis of ..:

Ungaro, C. ; Mazzei, R. ; Conforti, F.L....
Journal of Neuroscience Research.  87 (2009)  5 - p. 1162-1167 , 2009
Link: https://doi.org/10.1002/..
 
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13

A novel mutation in the X‐linked cyclin‐dependent kinase‐li..:

Sprovieri, T. ; Conforti, F.L. ; Fiumara, A....
American Journal of Medical Genetics Part A.  149A (2009)  4 - p. 722-725 , 2009
Link: https://doi.org/10.1002/..
 
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14

Brain‐derived neurotrophic factor and risk for primary adul..:

Martino, D. ; Muglia, M. ; Abbruzzese, G....
European Journal of Neurology.  16 (2009)  8 - p. 949-952 , 2009
Link: https://doi.org/10.1111/..
 
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15

A novel locus for dHMN with pyramidal features maps to chro..:

Muglia, M ; Magariello, A ; Citrigno, L...
Clinical Genetics.  73 (2008)  5 - p. 486-491 , 2008
Link: https://doi.org/10.1111/..
 
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