Response to "Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurological phenotype"

Salvatore Rossi; Alessia Perna; Anna Modoni; Enrico Bertini; Enrico Silvio Bertini; Vittorio Riso; Tommaso Filippo Nicoletti; Gabriella Silvestri

doi:10.1016/j.nmd.2020.01.003

Response to "Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurological phenotype"

Salvatore Rossi, Alessia Perna, Anna Modoni, Enrico Bertini, Enrico Silvio Bertini, Vittorio Riso, Tommaso Filippo Nicoletti, Gabriella Silvestri

IRCCS Ospedale pediatrico Bambino Gesù - Roma

Risultato della ricerca: Contributo in rivista › Articolo in rivista

1 Citazioni (Scopus)

Abstract

.

Lingua originale	English
pagine (da-a)	N/A-N/A
Rivista	Neuromuscular Disorders
DOI	https://doi.org/10.1016/j.nmd.2020.01.003
Stato di pubblicazione	Pubblicato - 2020

Keywords

ARAN-NM
HINT1
Neurodevelopmental
Psychiatric

Accesso al documento

10.1016/j.nmd.2020.01.003

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title = "Response to {"}Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurological phenotype{"}",

abstract = ".",

keywords = "ARAN-NM, HINT1, Neurodevelopmental, Psychiatric, ARAN-NM, HINT1, Neurodevelopmental, Psychiatric",

author = "Salvatore Rossi and Alessia Perna and Anna Modoni and Enrico Bertini and Bertini, {Enrico Silvio} and Vittorio Riso and Nicoletti, {Tommaso Filippo} and Gabriella Silvestri",

year = "2020",

doi = "10.1016/j.nmd.2020.01.003",

language = "English",

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journal = "Neuromuscular Disorders",

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TY - JOUR

T1 - Response to "Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurological phenotype"

AU - Rossi, Salvatore

AU - Perna, Alessia

AU - Modoni, Anna

AU - Bertini, Enrico

AU - Bertini, Enrico Silvio

AU - Riso, Vittorio

AU - Nicoletti, Tommaso Filippo

AU - Silvestri, Gabriella

PY - 2020

Y1 - 2020

N2 - .

AB - .

KW - ARAN-NM

KW - HINT1

KW - Neurodevelopmental

KW - Psychiatric

KW - ARAN-NM

KW - HINT1

KW - Neurodevelopmental

KW - Psychiatric

UR - http://hdl.handle.net/10807/150336

U2 - 10.1016/j.nmd.2020.01.003

DO - 10.1016/j.nmd.2020.01.003

M3 - Article

SN - 0960-8966

SP - N/A-N/A

JO - Neuromuscular Disorders

JF - Neuromuscular Disorders

ER -

Response to "Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurological phenotype"

Abstract

Keywords

Accesso al documento

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