المؤلفون: Veneziano, L, Parkinson, MH, Mantuano, E, Frontali, M, Bhatia, KP, Giunti, P

المصدر: Cerebellum , 13 (5) pp. 588-595. (2014)

مصطلحات موضوعية: Benign hereditary chorea, Ataxia, Hypothyroidism, Pituitary gland, Thyroid transcription factor 1

وصف الملف: application/pdf

العلاقة: https://discovery.ucl.ac.uk/id/eprint/1433196/1/art%253A10.1007%252Fs12311-014-0570-7.pdfTest; https://discovery.ucl.ac.uk/id/eprint/1433196Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/1433196/1/art%253A10.1007%252Fs12311-014-0570-7.pdfTest
https://discovery.ucl.ac.uk/id/eprint/1433196Test/

المؤلفون: Iodice A., Carecchio M., Zorzi G., Garavaglia B., Spagnoli C., Salerno G. G., Frattini D., Mencacci N. E., Invernizzi F., Veneziano L., Mantuano E., Angriman M., Fusco C.

المساهمون: Iodice, A., Carecchio, M., Zorzi, G., Garavaglia, B., Spagnoli, C., Salerno, G. G., Frattini, D., Mencacci, N. E., Invernizzi, F., Veneziano, L., Mantuano, E., Angriman, M., Fusco, C.

مصطلحات موضوعية: ADCY5, Benign hereditary chorea, Levodopa, NKX2-1-related chorea, Restless legs syndrome, Adult, Brain, Child, Preschool, Chorea, Cohort Studie, Dopamine Agent, Family Health, Female, Human, Magnetic Resonance Imaging, Male, Mutation, Pituitary Gland, Thyroid Nuclear Factor 1

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30352709; info:eu-repo/semantics/altIdentifier/wos/WOS:000462417200006; volume:41; issue:3; firstpage:250; lastpage:256; numberofpages:7; journal:BRAIN & DEVELOPMENT; http://hdl.handle.net/11577/3313758Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85055095313; www.elsevier.com/locate/braindev

الإتاحة: https://doi.org/10.1016/j.braindev.2018.10.001Test
http://hdl.handle.net/11577/3313758Test

المؤلفون: Veneziano L., Parkinson M.H., Mantuano E., Frontali M., Bhatia K.P., Giunti P.

المصدر: Cerebellum (Lond., Print) (2014). doi:10.1007/s12311-014-0570-7
info:cnr-pdr/source/autori:Veneziano L.; Parkinson M.H.; Mantuano E.; Frontali M.; Bhatia K.P.; Giunti P./titolo:A Novel De Novo Mutation of the TITF1%2FNKX2-1 Gene Causing Ataxia, Benign Hereditary Chorea, Hypothyroidism and a Pituitary Mass in a UK Family and Review of the Literature/doi:10.1007%2Fs12311-014-0570-7/rivista:Cerebellum (Lond., Print)/anno:2014/pagina_da:/pagina_a:/intervallo_pagine:/volume

مصطلحات موضوعية: Pituitary gland, congenital, hereditary, and neonatal diseases and abnormalities, Hypothyroidism, Thyroid transcription factor 1, Ataxia, Benign hereditary chorea

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=cnr_________::a0151e55be35da787bd6521faedacd0cTest
http://www.cnr.it/prodotto/i/281405Test