المؤلفون: Teles, J., Rivera-Ascona, C., Polli, R. S., Oliveira-Silva, R., Vidoto, E. L. G., Andreeta, J. P., Bonagamba, T. J.

مصطلحات موضوعية: Quantum Physics

URL الوصول: http://arxiv.org/abs/1404.0095

المؤلفون: Godler, DE, Ling, L, Gamage, D, Baker, EK, Bui, M, Field, MJ, Rogers, C, Butler, MG, Murgia, A, Leonardi, E, Polli, R, Schwartz, CE, Skinner, CD, Alliende, AM, Santa Maria, L, Pitt, J, Greaves, R, Francis, D, Oertel, R, Wang, M, Simons, C, Amor, DJ

Relation: pii: 2787581; Godler, D. E., Ling, L., Gamage, D., Baker, E. K., Bui, M., Field, M. J., Rogers, C., Butler, M. G., Murgia, A., Leonardi, E., Polli, R., Schwartz, C. E., Skinner, C. D., Alliende, A. M., Santa Maria, L., Pitt, J., Greaves, R., Francis, D., Oertel, R. ,. Amor, D. J. (2022). Feasibility of Screening for Chromosome 15 Imprinting Disorders in 16 579 Newborns by Using a Novel Genomic Workflow. JAMA NETWORK OPEN, 5 (1), https://doi.org/10.1001/jamanetworkopen.2021.41911.; http://hdl.handle.net/11343/307926

الاتاحة: http://hdl.handle.net/11343/307926

المؤلفون: Pascoal, V. D. B., Marchesini, R. B., Athié, M. C. P., Matos, A. H. B., Conte, F. F., Pereira, T. C., Secolin, R., Gilioli, R., Malheiros, J. M., Polli, R. S., Tannús, A., Covolan, L., Pascoal, L. B., Vieira, A. S., Cavalheiro, E. A., Cendes, F., Lopes-Cendes, I.

المساهمون: Fundação de Amparo à Pesquisa do Estado de São Paulo, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Conselho Nacional de Desenvolvimento Científico e Tecnológico

المصدر: Cellular and Molecular Neurobiology ; volume 43, issue 1, page 367-380 ; ISSN 0272-4340 1573-6830

الاتاحة: http://dx.doi.org/10.1007/s10571-022-01190-y
https://link.springer.com/content/pdf/10.1007/s10571-022-01190-y.pdf
https://link.springer.com/article/10.1007/s10571-022-01190-y/fulltext.html

المؤلفون: Jain S., Bakolitsa C., Brenner S. E., Radivojac P., Moult J., Repo S., Hoskins R. A., Andreoletti G., Barsky D., Chellapan A., Chu H., Dabbiru N., Kollipara N. K., Ly M., Neumann A. J., Pal L. R., Odell E., Pandey G., Peters-Petrulewicz R. C., Srinivasan R., Yee S. F., Yeleswarapu S. J., Zuhl M., Adebali O., Patra A., Beer M. A., Hosur R., Peng J., Bernard B. M., Berry M., Dong S., Boyle A. P., Adhikari A., Chen J., Hu Z., Wang R., Wang Y., Miller M., Bromberg Y., Turina P., Capriotti E., Han J. J., Ozturk K., Carter H., Babbi G., Bovo S., Di Lena P., Martelli P. L., Savojardo C., Casadio R., Cline M. S., De Baets G., Bonache S., Diez O., Gutierrez-Enriquez S., Fernandez A., Montalban G., Ootes L., Ozkan S., Padilla N., Riera C., De la Cruz X., Diekhans M., Huwe P. J., Wei Q., Xu Q., Dunbrack R. L., Gotea V., Elnitski L., Margolin G., Fariselli P., Kulakovskiy I. V., Makeev V. J., Penzar D. D., Vorontsov I. E., Favorov A. V., Forman J. R., Hasenahuer M., Fornasari M. S., Parisi G., Avsec Z., Celik M. H., Nguyen T. Y. D., Gagneur J., Shi F. -Y., Edwards M. D., Guo Y., Tian K., Zeng H., Gifford D. K., Goke J., Zaucha J., Gough J., Ritchie G. R. S., Frankish A., Mudge J. M., Harrow J., Young E. L., Yu Y., Huff C. D., Murakami K., Nagai Y., Imanishi T., Mungall C. J., Jacobsen J. O. B., Kim D., Jeong C. -S., Jones D. T., Li M. J., Guthrie V. B., Bhattacharya R., Chen Y. -C., Douville C., Fan J., Masica D., Niknafs N., Sengupta S., Tokheim C., Turner T. N., Yeo H. T. G., Karchin R., Shin S., Welch R., Keles S., Li Y., Kellis M., Corbi-Verge C., Strokach A. V., Kim P. M., Klein T. E., Mohan R., Sinnott-Armstrong N. A., Wainberg M., Kundaje A., Gonzaludo N., Mak A. C. Y., Chhibber A., Lam H. Y. K., Dahary D., Fishilevich S., Lancet D., Lee I., Bachman B., Katsonis P., Lua R. C., Wilson S. J., Lichtarge O., Bhat R. R., Sundaram L., Viswanath V., Bellazzi R., Nicora G., Rizzo E., Limongelli I., Mezlini A. M., Chang R., Kim S., Lai C., O'Connor R., Topper S., van den Akker J., Zhou A. Y., Zimmer A. D., Mishne G., Bergquist T. R., Breese M. R., Guerrero R. F., Jiang Y., Kiga N., Li B., Mort M., Pagel K. A., Pejaver V., Stamboulian M. H., Thusberg J., Mooney S. D., Teerakulkittipong N., Cao C., Kundu K., Yin Y., Yu C. -H., Kleyman M., Lin C. -F., Stackpole M., Mount S. M., Eraslan G., Mueller N. S., Naito T., Rao A. R., Azaria J. R., Brodie A., Ofran Y., Garg A., Pal D., Hawkins-Hooker A., Kenlay H., Reid J., Mucaki E. J., Rogan P. K., Schwarz J. M., Searls D. B., Lee G. R., Seok C., Kramer A., Shah S., Huang C. V., Kirsch J. F., Shatsky M., Cao Y., Chen H., Karimi M., Moronfoye O., Sun Y., Shen Y., Shigeta R., Ford C. T., Nodzak C., Uppal A., Shi X., Joseph T., Kotte S., Rana S., Rao A., Saipradeep V. G., Sivadasan N., Sunderam U., Stanke M., Su A., Adzhubey I., Jordan D. M., Sunyaev S., Rousseau F., Schymkowitz J., Van Durme J., Tavtigian S. V., Carraro M., Giollo M., Tosatto S. C. E., Adato O., Carmel L., Cohen N. E., Fenesh T., Holtzer T., Juven-Gershon T., Unger R., Niroula A., Olatubosun A., Valiaho J., Yang Y., Vihinen M., Wahl M. E., Chang B., Chong K. C., Hu I., Sun R., Wu W. K. K., Xia X., Zee B. C., Wang M. H., Wang M., Wu C., Lu Y., Chen K., Yates C. M., Kreimer A., Yan Z., Yosef N., Zhao H., Wei Z., Yao Z., Zhou F., Folkman L., Zhou Y., Daneshjou R., Altman R. B., Inoue F., Ahituv N., Arkin A. P., Lovisa F., Bonvini P., Bowdin S., Gianni S., Mantuano E., Minicozzi V., Novak L., Pasquo A., Pastore A., Petrosino M., Puglisi R., Toto A., Veneziano L., Chiaraluce R., Ball M. P., Bobe J. R., Church G. M., Consalvi V., Cooper D. N., Buckley B. A., Sheridan M. B., Cutting G. R., Scaini M. C., Cygan K. J., Fredericks A. M., Glidden D. T., Neil C., Rhine C. L., Fairbrother W. G., Alontaga A. Y., Fenton A. W., Matreyek K. A., Starita L. M., Fowler D. M., Loscher B. -S., Franke A., Adamson S. I., Graveley B. R., Gray J. W., Malloy M. J., Kane J. P., Kousi M., Katsanis N., Schubach M., Kircher M., Tang P. L. F., Kwok P. -Y., Lathrop R. H., Clark W. T., Yu G. K., LeBowitz J. H., Benedicenti F., Bettella E., Bigoni S., Cesca F., Mammi I., Marino-Buslje C., Milani D., Peron A., Polli R., Sartori S., Stanzial F., Toldo I., Turolla L., Aspromonte M. C., Bellini M., Leonardi E., Liu X., Marshall C., McCombie W. R., Elefanti L., Menin C., Meyn M. S., Murgia A., Nadeau K. C. Y., Neuhausen S. L., Nussbaum R. L., Pirooznia M., Potash J. B., Dimster-Denk D. F., Rine J. D., Sanford J. R., Snyder M., Cote A. G., Sun S., Verby M. W., Weile J., Roth F. P., Tewhey R., Sabeti P. C., Campagna J., Refaat M. M., Wojciak J., Grubb S., Schmitt N., Shendure J., Spurdle A. B., Stavropoulos D. J., Walton N. A., Zandi P. P., Ziv E., Burke W., Chen F., Carr L. R., Martinez S., Paik J., Harris-Wai J., Yarborough M., Fullerton S. M., Koenig B. A., McInnes G., Shigaki D., Chandonia J. -M., Furutsuki M., Kasak L., Yu C., Chen R., Friedberg I., Getz G. A., Cong Q., Kinch L. N., Zhang J., Grishin N. V., Voskanian A., Kann M. G., Tran E., Ioannidis N. M., Hunter J. M., Udani R., Cai B., Morgan A. A., Sokolov A., Stuart J. M., Minervini G., Monzon A. M., Batzoglou S., Butte A. J., Greenblatt M. S., Hart R. K., Hernandez R., Hubbard T. J. P., Kahn S., O'Donnell-Luria A., Ng P. C., Shon J., Veltman J., Zook J. M.

المساهمون: Jain, S., Bakolitsa, C., Brenner, S. E., Radivojac, P., Moult, J., Repo, S., Hoskins, R. A., Andreoletti, G., Barsky, D., Chellapan, A., Chu, H., Dabbiru, N., Kollipara, N. K., Ly, M., Neumann, A. J., Pal, L. R., Odell, E., Pandey, G., Peters-Petrulewicz, R. C., Srinivasan, R., Yee, S. F., Yeleswarapu, S. J., Zuhl, M., Adebali, O., Patra, A., Beer, M. A., Hosur, R., Peng, J., Bernard, B. M., Berry, M., Dong, S., Boyle, A. P., Adhikari, A., Chen, J., Hu, Z., Wang, R., Wang, Y., Miller, M., Bromberg, Y., Turina, P., Capriotti, E., Han, J. J., Ozturk, K., Carter, H., Babbi, G., Bovo, S., Di Lena, P., Martelli, P. L., Savojardo, C., Casadio, R., Cline, M. S., De Baets, G., Bonache, S., Diez, O., Gutierrez-Enriquez, S., Fernandez, A., Montalban, G., Ootes, L., Ozkan, S., Padilla, N., Riera, C., De la Cruz, X., Diekhans, M., Huwe, P. J., Wei, Q., Xu, Q., Dunbrack, R. L., Gotea, V., Elnitski, L., Margolin, G., Fariselli, P., Kulakovskiy, I. V., Makeev, V. J., Penzar, D. D., Vorontsov, I. E., Favorov, A. V., Forman, J. R., Hasenahuer, M., Fornasari, M. S., Parisi, G., Avsec, Z., Celik, M. H., Nguyen, T. Y. D., Gagneur, J., Shi, F. -Y., Edwards, M. D., Guo, Y., Tian, K., Zeng, H., Gifford, D. K., Goke, J., Zaucha, J., Gough, J., Ritchie, G. R. S., Frankish, A., Mudge, J. M., Harrow, J., Young, E. L., Yu, Y.

مصطلحات موضوعية: Variant detection, bioinformatics

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/pmid/38389099; volume:25; issue:1; journal:GENOME BIOLOGY; https://hdl.handle.net/11571/1498598; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85187866396; https://genomebiology.biomedcentral.com/articles/10.1186/s13059-023-03113-6

الاتاحة: https://hdl.handle.net/11571/1498598
https://doi.org/10.1186/s13059-023-03113-6
https://genomebiology.biomedcentral.com/articles/10.1186/s13059-023-03113-6

المؤلفون: Leonardi E., Bettella E., Pelizza M. F., Aspromonte M. C., Polli R., Boniver C., Sartori S., Milani D., Murgia A.

المساهمون: Leonardi, E., Bettella, E., Pelizza, M. F., Aspromonte, M. C., Polli, R., Boniver, C., Sartori, S., Milani, D., Murgia, A.

مصطلحات موضوعية: epilepsy, epileptic encephalopathy, gene panel, ID, MRD29, NGS, SETBP1

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/33391157; info:eu-repo/semantics/altIdentifier/wos/WOS:000603374400001; volume:11; firstpage:1; lastpage:10; numberofpages:10; journal:FRONTIERS IN NEUROLOGY; http://hdl.handle.net/11577/3391275; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85098481915

الاتاحة: http://hdl.handle.net/11577/3391275
https://doi.org/10.3389/fneur.2020.593446

المؤلفون: Leonardi E., Bellini M., Aspromonte M. C., Polli R., Mercante A., Ciaccio C., Granocchio E., Bettella E., Donati I., Cainelli E., Boni S., Sartori S., Pantaleoni C., Boniver C., Murgia A.

المساهمون: Leonardi, E., Bellini, M., Aspromonte, M. C., Polli, R., Mercante, A., Ciaccio, C., Granocchio, E., Bettella, E., Donati, I., Cainelli, E., Boni, S., Sartori, S., Pantaleoni, C., Boniver, C., Murgia, A.

مصطلحات موضوعية: ASD, Epilepsy, ESES, Gene panel, ID, Mosaicism, NGS, WAC

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/pmid/32214004; info:eu-repo/semantics/altIdentifier/wos/WOS:000529189000108; volume:11; issue:3; firstpage:344; numberofpages:16; journal:GENES; http://hdl.handle.net/11577/3340470; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85082481693; https://www.mdpi.com/2073-4425/11/3/344

الاتاحة: http://hdl.handle.net/11577/3340470
https://doi.org/10.3390/genes11030344
https://www.mdpi.com/2073-4425/11/3/344

المؤلفون: Aspromonte M. C., BELLINI, MARIAGRAZIA, Gasparini A., Carraro M., Bettella E., Polli R., Cesca F., Bigoni S., Boni S., Carlet O., Negrin S., Mammi I., MILANI, DUCCIO, Peron A., Sartori S., Toldo I., Soli F., Turolla L., Stanzial F., Benedicenti F., MARINO BUSLJE, CRISTINA ESTER, Tosatto S. C. E., Murgia A., Leonardi E.

المساهمون: Aspromonte, M. C., Bellini, Mariagrazia, Gasparini, A., Carraro, M., Bettella, E., Polli, R., Cesca, F., Bigoni, S., Boni, S., Carlet, O., Negrin, S., Mammi, I., Milani, Duccio, Peron, A., Sartori, S., Toldo, I., Soli, F., Turolla, L., Stanzial, F., Benedicenti, F., MARINO BUSLJE, CRISTINA ESTER, Tosatto, S. C. E., Murgia, A., Leonardi, E.

مصطلحات موضوعية: ASD, ID, NGS, comorbidity, gene panel, variant interpretation

Relation: info:eu-repo/semantics/altIdentifier/pmid/31209962; info:eu-repo/semantics/altIdentifier/wos/WOS:000479853400001; journal:HUMAN MUTATION; http://hdl.handle.net/11577/3307129; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85070077996

الاتاحة: http://hdl.handle.net/11577/3307129
https://doi.org/10.1002/humu.23822

المؤلفون: Vera, G, Sorlin, A, Delplancq, G, Lecoquierre, F, Brasseur-Daudruy, M, Petit, F, Smol, T, Ziegler, A, Bonneau, D, Colin, E, Mercier, S, Cogné, B, Bézieau, S, Edery, P, Lesca, G, Chatron, N, Sabatier, I, Duban-Bedu, B, Colson, C, Piton, A, Durand, B, Capri, Y, Perrin, L, Wiesener, A, Zweier, C, Maroofian, R, Carroll, CJ, Galehdari, H, Mazaheri, N, Callewaert, B, Giulianno, F, Zaafrane-Khachnaoui, K, Buchert-Lo, R, Haack, T, Magg, J, Rieß, A, Blandfort, M, Waldmüller, S, Horber, V, Leonardi, E, Polli, R, Turolla, L, Murgia, A, Frebourg, T, Lebre, AS, Nicolas, G, Saugier-Veber, P, Guerrot, AM

المصدر: European Journal of Medical Genetics , 63 (10) , Article 104004. (2020)

مصطلحات موضوعية: Developmental delay, GATAD2B, Intellectual disability, Next-generation sequencing, Adolescent, Adult, Brain, Child, Preschool, Face, Female, GATA Transcription Factors, High-Throughput Nucleotide Sequencing, Humans, Infant, Magnetic Resonance Imaging, Male, Megalencephaly, Muscle Hypotonia, Neurodevelopmental Disorders, Phenotype, Pregnancy, Repressor Proteins, Sequence Deletion, Speech Disorders

وصف الملف: text

Relation: https://discovery.ucl.ac.uk/id/eprint/10146514/1/1-s2.0-S1769721220305073-am.pdf; https://discovery.ucl.ac.uk/id/eprint/10146514/

الاتاحة: https://discovery.ucl.ac.uk/id/eprint/10146514/1/1-s2.0-S1769721220305073-am.pdf
https://discovery.ucl.ac.uk/id/eprint/10146514/

المؤلفون: Sawacha Z., Spolaor F., Piatkowska W. J., Cibin F., Ciniglio A., Guiotto A., Ricca M., Polli R., Murgia A.

المساهمون: Sawacha, Z., Spolaor, F., Piatkowska, W. J., Cibin, F., Ciniglio, A., Guiotto, A., Ricca, M., Polli, R., Murgia, A.

مصطلحات موضوعية: Fragile X syndrome, Gait analysi, Kinematic, Surface electromyography, Biomechanical Phenomena, Child, Electromyography, Feasibility Studie, Human, Range of Motion, Articular, Reproducibility of Result, Gait, Muscle, Skeletal

Relation: info:eu-repo/semantics/altIdentifier/pmid/34300485; info:eu-repo/semantics/altIdentifier/wos/WOS:000677013000001; volume:21; issue:14; firstpage:4746; journal:SENSORS; http://hdl.handle.net/11577/3406848; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85109555525

الاتاحة: http://hdl.handle.net/11577/3406848
https://doi.org/10.3390/s21144746

المؤلفون: Ciaccio C., Leonardi E., Polli R., Murgia A., D'Arrigo S., Granocchio E., Chiapparini L., Pantaleoni C., Esposito S.

المساهمون: Ciaccio, C., Leonardi, E., Polli, R., Murgia, A., D'Arrigo, S., Granocchio, E., Chiapparini, L., Pantaleoni, C., Esposito, S.

مصطلحات موضوعية: cerebellar hypoplasia, developmental delay, developmental disorder, KIRREL3, pediatric ataxia

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/pmid/33853164; info:eu-repo/semantics/altIdentifier/wos/WOS:000640005900005; journal:NEUROPEDIATRICS; http://hdl.handle.net/11577/3391288; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85104381200

الاتاحة: http://hdl.handle.net/11577/3391288
https://doi.org/10.1055/s-0041-1725964

المؤلفون: Pascoal, V. D. B., Marchesini, R. B., Athié, M. C. P., Matos, A. H. B., Conte, F. F., Pereira, T. C., Secolin, R., Gilioli, R., Malheiros, J. M., Polli, R. S., Tannús, A., Covolan, L., Pascoal, L. B., Vieira, A. S., Cavalheiro, E. A., Cendes, F., Lopes-Cendes, I.

المصدر: Cellular & Molecular Neurobiology; Jan2023, Vol. 43 Issue 1, p367-380, 14p

مصطلحات موضوعية: TEMPORAL lobe epilepsy, CENTRAL nervous system, EPILEPSY, ANIMAL mortality, PILOCARPINE, CEREBRAL edema

المؤلفون: SARTORI, STEFANO, TOLDO, IRENE, CASARIN, ALBERTO, DRIGO, PAOLA, MURGIA, ALESSANDRA, ANESI L, POLLI R

المساهمون: Sartori, Stefano, Anesi, L, Polli, R, Toldo, Irene, Casarin, Alberto, Drigo, Paola, Murgia, Alessandra

مصطلحات موضوعية: Angelman syndrome, mutation, phenotype, splice-site, UBE3A

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000257956300010; volume:23; firstpage:912; lastpage:915; journal:JOURNAL OF CHILD NEUROLOGY; http://hdl.handle.net/11577/2459073; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-48449085507

الاتاحة: http://hdl.handle.net/11577/2459073
https://doi.org/10.1177/0883073808316367

المؤلفون: Cesca F., Bettella E., Polli R., Leonardi E., Aspromonte M. C., Sicilian B., Stanzial F., Benedicenti F., Sensi A., Ciorba A., Bigoni S., Cama E., Scimemi P., Santarelli R., Murgia A.

المساهمون: Cesca, F., Bettella, E., Polli, R., Leonardi, E., Aspromonte, M. C., Sicilian, B., Stanzial, F., Benedicenti, F., Sensi, A., Ciorba, A., Bigoni, S., Cama, E., Scimemi, P., Santarelli, R., Murgia, A.

مصطلحات موضوعية: Adolescent, Adult, Cadherin, Child, Preschool, Connexin 26, Connexin 30, Deafne, Female, Genetic Association Studie, Hearing Loss, Sensorineural, High-Throughput Nucleotide Sequencing, Human, Male, Phenotype, Usher Syndrome, Young Adult, Genetic Heterogeneity, Mutation

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/32467589; info:eu-repo/semantics/altIdentifier/wos/WOS:000536074300001; volume:65; issue:10; firstpage:855; lastpage:864; journal:JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/11577/3342974; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85085478685

الاتاحة: http://hdl.handle.net/11577/3342974
https://doi.org/10.1038/s10038-020-0783-1

المؤلفون: Sawacha Z., Spolaor F., Piatkowska W., Cibin F., Pavan D., Guiotto A., Polli R., Ricca M., Murgia A.

المساهمون: Sawacha, Z., Spolaor, F., Piatkowska, W., Cibin, F., Pavan, D., Guiotto, A., Polli, R., Ricca, M., Murgia, A.

وصف الملف: ELETTRONICO

Relation: volume:81; firstpage:329; lastpage:330; numberofpages:2; journal:GAIT & POSTURE; http://hdl.handle.net/11577/3378093

الاتاحة: http://hdl.handle.net/11577/3378093
https://doi.org/10.1016/j.gaitpost.2020.08.061

المؤلفون: Piatkowska W, Sawacha Z, Spolaor F, Romanato M, Voltan S, Cibin F, Pavan D, Guiotto A, Polli R, Murgia A

المساهمون: Piatkowska, W, Sawacha, Z, Spolaor, F, Romanato, M, Voltan, S, Cibin, F, Pavan, D, Guiotto, A, Polli, R, Murgia, A

وصف الملف: ELETTRONICO

Relation: volume:81; firstpage:269; lastpage:270; numberofpages:2; journal:GAIT & POSTURE; http://hdl.handle.net/11577/3378098

الاتاحة: http://hdl.handle.net/11577/3378098
https://doi.org/10.1016/j.gaitpost.2020.08.030

المؤلفون: Sawacha, Z., Spolaor, F., Cibin, F., Piatkowska, W., Pavan, D., Guiotto, A., Polli, R., Ricca, M., Murgia, A.

المساهمون: Sawacha, Z., Spolaor, F., Cibin, F., Piatkowska, W., Pavan, D., Guiotto, A., Polli, R., Ricca, M., Murgia, A.

وصف الملف: ELETTRONICO

Relation: volume:74; firstpage:35; lastpage:36; numberofpages:2; journal:GAIT & POSTURE; http://hdl.handle.net/11577/3333353

الاتاحة: http://hdl.handle.net/11577/3333353
https://doi.org/10.1016/j.gaitpost.2019.07.495

المؤلفون: Murgia, A, Orzan, E, Polli, R, Martella, M, Vinanzi, C, Leonardi, E, Arslan, E, Zacchello, F

مصطلحات موضوعية: Original articles

وصف الملف: text/html

Relation: http://jmg.bmj.com/cgi/content/short/36/11/829; http://dx.doi.org/10.1136/jmg.36.11.829

الاتاحة: http://jmg.bmj.com/cgi/content/short/36/11/829
https://doi.org/10.1136/jmg.36.11.829

المؤلفون: Orzan, E., Polli, R., Martella, M., Vinanzi, C., Leonardi, M., Murgia, A.

المصدر: British Journal of Audiology ; volume 33, issue 5, page 291-295 ; ISSN 0300-5364

الاتاحة: http://dx.doi.org/10.3109/03005369909090112
http://www.tandfonline.com/doi/pdf/10.3109/03005369909090112

المؤلفون: Sawacha, Z., Spolaor, F., Cibin, F., Slasko, W., Pavan, D., Guiotto, A., Polli, R., Ricca, M., Murgia, A.

المصدر: Gait & Posture ; ISSN 0966-6362

الاتاحة: http://dx.doi.org/10.1016/j.gaitpost.2019.07.435
https://api.elsevier.com/content/article/PII:S0966636219312469?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0966636219312469?httpAccept=text/plain

المؤلفون: Carson, Mary C, Breslyn, Wayne, Carmany, J, Cross, S, Farrington, W H, Hahn, A, Jaworski, J, Lansdon, P, Li, M, Pearson, D, Polli, R, Shepherd, E, Singh, D, Sundlof, S, Tieso, T, Wagner, R, Wentworth, J, Wilson, B

المصدر: Journal of AOAC INTERNATIONAL ; volume 79, issue 1, page 29-42 ; ISSN 1060-3271 1944-7922

الاتاحة: http://dx.doi.org/10.1093/jaoac/79.1.29
http://academic.oup.com/jaoac/article-pdf/79/1/29/32468072/jaoac0029.pdf