Zobrazeno 1 - 10
of 1 113
pro vyhledávání: '"Ajmar F"'
Autor:
Gasparini, P., Mandich, P., Novelli, G., Bellone, E., Sangiuolo, F., De Stefano, F., Potenza, L., Trabetti, E., Marigo, M., Pignatti, P.F., Dallapiccola, B., Ajmar, F.
Publikováno v:
Human Heredity, 1991 Jan 01. 41(3), 174-181.
Externí odkaz:
https://www.jstor.org/stable/45102418
Autor:
Pigullo, S, DI MARIA, E, Marchese, R, Assini, A, Bellone, E, Scaglione, C, Vitale, C, Bonuccelli, U, Barone, Paolo, Ajmar, F, Martinelli, P, Abbruzzese, G.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2e6c7622197a67fe3575c662bfe6f490
http://hdl.handle.net/11588/131740
http://hdl.handle.net/11588/131740
Autor:
Sheth, Jayesh1 (AUTHOR) jayesh.sheth@frige.co.in, Nair, Aadhira1 (AUTHOR), Sheth, Frenny1 (AUTHOR), Ajagekar, Manali1 (AUTHOR), Dhondekar, Tejasvi1 (AUTHOR), Panigrahi, Inusha2 (AUTHOR), Bavdekar, Ashish3 (AUTHOR), Nampoothiri, Sheela4 (AUTHOR), Datar, Chaitanya5 (AUTHOR), Gandhi, Ajit6 (AUTHOR), Muranjan, Mamta7 (AUTHOR), Kaur, Anupriya2 (AUTHOR), Desai, Manisha1 (AUTHOR), Mistri, Mehul1 (AUTHOR), Patel, Chitra1 (AUTHOR), Naik, Premal8 (AUTHOR), Shah, Maulin9 (AUTHOR), Godbole, Koumudi10 (AUTHOR), Kapoor, Seema11 (AUTHOR), Gupta, Neerja12 (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 8/13/2024, Vol. 19 Issue 1, p1-17. 17p.
Autor:
Pigullo, S, De Luca, A, Barone, P, Marchese, R, Bellone, E, Colosimo, A, Scaglione, C, Martinelli, P, Di Maria, E, Pizzuti, Antonio, Abbruzzese, G, Dallapiccola, B, Ajmar, F, Mandich, P.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3686::d05ce69799a2ed1ebdf8bb65764e5c12
http://hdl.handle.net/11573/116895
http://hdl.handle.net/11573/116895
Autor:
Pigullo, S, Di Maria, E, Marchese, R, Bellone, E, Gulli, R, Scaglione, C, Battaglia, S, Barone, Paolo, Martinelli, P, Abbruzzese, G, Ajmar, F, Mandich, P.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8cc6699c989c8ceff90f599b004915fd
http://hdl.handle.net/11567/250576
http://hdl.handle.net/11567/250576
Autor:
Origone, P., Luca, A., Bellini, C., Buccino, A., Mingarelli, R., Costabel, S., La Rosa, C., Garrè, C., Coviello, D. A., Ajmar, F., Bruno Dallapiccola, Bonioli, E.
Publikováno v:
Scopus-Elsevier
The entire NF1 coding region was analyzed for mutations in a panel of 108 unrelated Italian NF1 patients. Using PTT, SSCP, and DNA sequencing, we found 10 mutations which have never been reported before. Clinical diagnosis of NF1 was established acco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::238c167d81e56c425313e814059c314a
https://pubmed.ncbi.nlm.nih.gov/12112660
https://pubmed.ncbi.nlm.nih.gov/12112660
Autor:
Gulli, R, Pioli, R, De Luca, A, Begni, S, Pasini, A, Spalletta, G, Bellone, E, Pizzuti, A, Novelli, G, Dallapiccola, B, Ajmar, F, Gennarelli, Massimo, Mandich, P, Di Maria, E.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3662::1a32cdd9557fbfd1e208d36429c61eb0
http://hdl.handle.net/11379/72048
http://hdl.handle.net/11379/72048
Autor:
Abbruzzese, G, Pigullo, S, Di Maria, E, Martinelli, P, Barone, Paolo, Marchese, R, Scaglione, C, Assini, A, Lucetti, C, Berardelli, A, Calzetti, S, Bellone, E, Ajmar, F, Mandich, P.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3666::1d6173ae291ade92823812545da6842e
http://hdl.handle.net/11386/3358877
http://hdl.handle.net/11386/3358877