Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Hamida, Mongi Ben"'
Autor:
Othmane, Kamel Ben, Johnson, Ellen, Menold, Marisa, Graham, Felicia L., Hamida, Mongi Ben, Hasegawa, Osamu, Rogala, Allison D., Ohnishi, Akio, Pericak-Vance, Margaret, Hentati, Faycal, Vance, Jeffery M.
Publikováno v:
In Genomics 15 December 1999 62(3):344-349
Autor:
Diagana, Mohamadou, Druet-Cabanac, Michel, Macharia, Waruingi, Kabore, Jean, Avode Dossou, Gilbert, Grunitzky, Eric G., Kouassi, Ernest Beugré, Traore, Moussa, Condet, Ansoumame, Nzisabira, Leopold, Dumas, Michel, Allard, Michel, Preux, Pierre-Marie, Hamida, Mongi Ben
Publikováno v:
African Journal of Neurological Sciences; Vol 22, No 2 (2003)
Background The results of many public health programs carried out in many countries of the African continent have shown that the proportion of the elderly population within the African population will increase. Knowing the factors which will contribu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=78975075580c::900ed20c1459ea8cb7b820994196cf91
https://www.ajol.info/index.php/ajns/article/view/7536
https://www.ajol.info/index.php/ajns/article/view/7536
Autor:
Doerflinger, Nathalie, Linder, Catherine, Ouahchi, Karim, Gyapay, Gabor, Weissenbach, Jean, Le Paslier, Denis, Rigault, Philippe, Belal, Samir, Hamida, Christiane Ben, Hentati, Faycal, Hamida, Mongi Ben, Pandolfo, Massimo, DiDonato, Stephano, Sokol, Ronald, Kayden, Herbert, Landrieu, Pierre, Durr, Alexandra, Brice, Alexis, Goutières, Françoise, Kohlschütter, Alfried, Sabouraud, Pascal, Benomar, Ali, Yahyaoui, Mohamed, Mandel, Jean-Louis, Koenig, Michel
Ataxia with vitamin E deficiency (AVED) is an autosomal recessive disease characterized clinically by neurological symptoms with often striking resemblance to those of Friedreich ataxia. This disorder has been reported previously as familial isolated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dd485c72f9e9f4566133155da1af142d
https://europepmc.org/articles/PMC1801469/
https://europepmc.org/articles/PMC1801469/
Autor:
Cavalier, Laurent, BenHamida, Christiane, Amouri, Rim, Belal, Samir, Bomont, Pascale, Lagarde, Nadège, Gressin, Laëtitia, Callen, David, Demir, Ercan, Topaloglu, Haluk, Landrieu, Pierre, Ioos, Catherine, Hamida, Mongi Ben, Kœnig, Michel, Hentati, Fayçal
Publikováno v:
European Journal of Human Genetics; Jul2000, Vol. 8 Issue 7, p527, 8p
Autor:
Nicole, Sophie, Hamida, Christiane Ben, Beighton, Peter, Bakouri, Selim, Belal, Samir, Romero, Norma, Viljoen, Denis, Ponsot, Gérard, Sammoud, Azza, Weissenbach, Jean, Fardeau, Michel, Hamida, Mongi Ben, Fontaine, Bertrand, Hentati, Fayçal
Publikováno v:
Human Molecular Genetics; Sep1995, Vol. 4 Issue 9, p1633-1636, 4p
Autor:
Hentati, Afif, Pericak-Vance, Margaret A., Lennon, Felicia, Wasserman, Brad, Hentati, Faycal, Juneja, Tony, Angrist, Misha H., Hung, Wu-Yen, Boustany, Rose-Mary, Bohlega, Saeed, Iqbal, Zafar, Huether, Carl H., Hamida, Mongi Ben, Siddique, Teepu
Publikováno v:
Human Molecular Genetics; Oct1994, Vol. 3 Issue 10, p1867-1871, 5p
Autor:
Hamida, Christiane Ben, Soussi-Yanicostas, Nadia, Butler-Browne, Gillian S., Bejaoui, Khemissa, Hentati, Fayçal, Hamida, Mongi Ben
Publikováno v:
Muscle & Nerve; 1994, Vol. 17 Issue 4, p400-410, 11p
Autor:
Hamida, Mongi Ben, Hentati, Fayçal, Schady, W., Meara, R. J., England, John D., Sumner, Austin J., Fishbein, William N., Sinkeler, S. P. T., Oh, Shin J., Hurwitz, Elliott L., Lee, Kwang W., Chang, Chien W., Cho, Hyo K., Entrikin, Richard K., Abresch, Richard T., Reininghaus, Jutta, Jockusch, Harald
Publikováno v:
Muscle & Nerve; 1989, Vol. 12 Issue 2, p156-163, 8p
Autor:
Hosler, Betsy A., Sapp, Peter C., Berger, Ralph, O'Neill, Gilmore, Bejaoui, Khemissa, Hamida, Mongi Ben, Hentati, Faycal, Chin, Wendy, McKenna-Yasek, Diane, Haines, Jonathan L., Patterson, David, Horvitz, H. Robert, Brown Jr., R. H., Day, C. B.
Publikováno v:
Neurogenetics; Dec1998, Vol. 2 Issue 1, p34-42, 9p
Publikováno v:
Brain: A Journal of Neurology; Mar1990, Vol. 113 Issue 2, p347-363, 17p