المؤلفون: Martinuzzi, A., Crippa, F., Panzeri, C., Arnoldi, A., Redaelli, F., Tonelli, A., Baschirotto, C., Mostacciuolo, Ml, Daga, A., D Angelo, Mg, Profice, P., Comi, G., Galbiati, S., Lamperti, C., Pandolfo, M., Meola, G., Musumeci, O., Toscano, A., Trevisan, C., Bresolin, N., Maria Teresa Bassi

المصدر: ResearcherID

مصطلحات موضوعية: SPG4 gene, Settore MED/26 - Neurologia, hereditary spastic paraplegia

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::55158621ef78369aa72dfa7140c731e8Test
http://hdl.handle.net/2434/32460Test

المؤلفون: Saad FA, Vitiello L, Mostacciuolo ML, Danieli G.A., OLIVIERO, Salvatore

المساهمون: Saad FA, Vitiello L, Oliviero S, Mostacciuolo ML, Danieli GA.

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:A1993LX65900011; volume:3; firstpage:60; lastpage:62; numberofpages:3; journal:PCR METHODS AND APPLICATIONS; http://hdl.handle.net/2318/141092Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0027197469

الإتاحة: http://hdl.handle.net/2318/141092Test

المؤلفون: Vitiello L, Mostacciuolo ML, Schiavon F, Nicoletti L, Angelini C, Danieli G.A., OLIVIERO, Salvatore

المساهمون: Vitiello L, Mostacciuolo ML, Oliviero S, Schiavon F, Nicoletti L, Angelini C, Danieli GA.

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:A1992HC71700012; volume:29; firstpage:127; lastpage:130; numberofpages:4; journal:JOURNAL OF MEDICAL GENETICS; http://hdl.handle.net/2318/141199Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0026535359

الإتاحة: http://hdl.handle.net/2318/141199Test

المؤلفون: Saad FA, Vitiello L, Merlini L, Mostacciuolo ML, Danieli G.A., OLIVIERO, Salvatore

المساهمون: Saad FA, Vitiello L, Merlini L, Mostacciuolo ML, Oliviero S, Danieli GA.

العلاقة: volume:1; firstpage:345; lastpage:346; numberofpages:2; journal:HUMAN MOLECULAR GENETICS; http://hdl.handle.net/2318/141070Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0026907070

الإتاحة: http://hdl.handle.net/2318/141070Test

المؤلفون: Kress W, Müller E, Kausch K, Kullmann F, Mostacciuolo ML, Rietschel M, Rotthauwe HW, Schmalenberger B, Voit T., SICILIANO, GABRIELE

المساهمون: Kress, W, Müller, E, Kausch, K, Kullmann, F, Mostacciuolo, Ml, Rietschel, M, Rotthauwe, Hw, Schmalenberger, B, Siciliano, Gabriele, Voit, T.

وصف الملف: STAMPA

العلاقة: volume:2; issue:2; firstpage:111; lastpage:115; numberofpages:5; journal:NEUROMUSCULAR DISORDERS; http://hdl.handle.net/11568/18194Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0026799360

الإتاحة: http://hdl.handle.net/11568/18194Test

المؤلفون: Siciliano, G, Manca, ML, Gennarelli, M, Angelini, C, Rocchi, A, Iudice, A, Miorin, M, Mostacciuolo, ML

المصدر: Clinical Genetics ; volume 59, issue 5, page 344-349 ; ISSN 0009-9163 1399-0004

الإتاحة: https://doi.org/10.1034/j.1399-0004.2001.590508.xTest

المؤلفون: Milani, M, Milani, N, Pareyson, D, Gorni, K, Merlini, L, Mostacciuolo, ML, Taroni, F.

المصدر: Journal of the Peripheral Nervous System ; volume 6, issue 1, page 52-53 ; ISSN 1085-9489 1529-8027

الإتاحة: https://doi.org/10.1046/j.1529-8027.2001.01007-36.xTest

المؤلفون: Saad, Fa, Mostacciuolo, Ml, Trevisan, Cp, Tomelleri, G, Angelini, C, Abdel Salam, E, Danieli, Ga

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od______3657::7d5d629f361cad89acf00e6c53b1c7b9Test
http://hdl.handle.net/11577/3355102Test

المؤلفون: Nelis, E., Broeckhoven, C., Jonghe, P., Lofgren, A., Vandenberghe, A., Latour, P., Le Guern, E., Brice, A., Mostacciuolo, Ml, Schiavon, F., Francesc Palau, Bort, S., Upadhyaya, M., Rocchi, M., Archidiacono, N., Mandich, P., Bellone, E., Silander, K., Savontaus, Ml, Navon, R., Goldberg-Stern, H., Estivill, X., Volpini, V., Friedl, W., Gal, A.

المصدر: European Journal of Human Genetics, 4, 25-33
European Journal of Human Genetics, 4, pp. 25-33
ResearcherID

مصطلحات موضوعية: X Chromosome, Charcot-Marie-Tooth Disease, epidemiology/genetics, Chromosomes, Human, Pair 17, Connexins, genetics, Europe, Gene Deletion, Gene Frequency, Genetic Testing, Hereditary Sensory and Motor Neuropathy, epidemiology/genetics, Humans, Multigene Family, Mutation, Myelin P0 Protein, genetics, Myelin Proteins, genetics, X Chromosome, Clinical description and delineation of genetic syndromes, medicine.disease_cause, Chromosomes, Connexins, Myelin, Onderzoek naar de pathogenese van de hereditaire neuropathieen CMT1a en HNPP, Gene Frequency, Peripheral myelin protein 22, Gene duplication, Genetics, Medicine, Humans, Genetic Testing, education, Klinische beschrijving en moleculaire definiëring van genetische syndromen, Gene, Genetics (clinical), education.field_of_study, Mutation, epidemiology/genetics, business.industry, Pair 17, Myelin protein zero, Chromosome, Europe, medicine.anatomical_structure, Multigene Family, Connexin 32, business, Hereditary Sensory and Motor Neuropathy, Myelin P0 Protein, Pathogenesis of the hereditary neuropathies CMT1a and HNPP, Gene Deletion, Myelin Proteins, Chromosomes, Human, Pair 17

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a80561e3ddba758a2d7a4a68899b8ffcTest
http://hdl.handle.net/2066/188335Test

المؤلفون: Boaretto F, Vettori A, Casarin A, Vazza G, Muglia M, Rossetto MG, Cavallaro T, Rizzuto N, Carelli V, Salviati L, Mostacciuolo ML, Martinuzzi A, Boaretto, F, Vettori, A, Casarin, A, Vazza, G, Muglia, M, Rossetto, M G, Cavallaro, T, Rizzuto, N

المصدر: Neurology; 6/8/2010, Vol. 74 Issue 23, p1919-1921, 3p