Výsledky vyhledávání - Guinto, Cheick O.
- Zobrazuji výsledky 1 - 11 z 11
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1
Fahr's syndrome with hyperparathyroidism revealed by seizures and proximal weakness Autor Dembélé, Kékouta, Cissé, Lassana, Djimdé, Samba, Coulibaly, Youlouza, Diarra, Salimata, Yalcouyé, Abdoulaye, Maiga, Boubacar, Guinto, Cheick O., Landouré, Guida
Vydáno 2019Text -
2
Neurological complications in subjects with sickle cell disease or trait in Mali Autor Landouré, Guida, Cissé, Lassana, Touré, Boubacar A, Yalcouyé, Abdoulaye, Coulibaly, Toumany, Sissoko, Adama S., Coulibaly, Thomas, Wonkam, Ambroise, Guinto, Cheick O.
Vydáno 2017Text -
3
A novel variant in the spatacsin gene causing SPG11 in a Malian family Autor Landouré, Guida, Dembélé, Kékouta, Cissé, Lassana, Diarra, Salimata, Samassékou, Oumar, Bocoum, Abdoulaye, Yalcouyé, Abdoulaye, Traoré, Moussa, Fischbeck, Kenneth H., Guinto, Cheick O.
Vydáno 2020Text -
4
Clinical and Genetic Analysis of Spinocerebellar Ataxia in Mali Autor Traoré, Moussa, Coulibaly, Toumany, Meilleur, Kathy G, La Pean, Alison, Sangaré, Modibo, Landouré, Guida, Mochel, Fanny, Karambé, Mamadou, Guinto, Cheick O, Fischbeck, Kenneth H
Vydáno 2011Text -
5
A novel mutation in the GARS gene in a Malian family with Charcot‐Marie‐Tooth disease Autor Yalcouyé, Abdoulaye, Diallo, Seybou H., Coulibaly, Thomas, Cissé, Lassana, Diallo, Salimata, Samassékou, Oumar, Diarra, Salimata, Coulibaly, Dramane, Keita, Mohamed, Guinto, Cheick O., Fischbeck, Kenneth, Landouré, Guida
Vydáno 2019Text -
6
Socio-cultural adaptation and standardization of Dubois' five words testing in a population of normal subject in Mali, West Africa Autor Guinto, Cheick O., Coulibaly, Toumany, Koné, Zeinab, Coulibaly, Souleymane, Maiga, Boubacar, Dembélé, Kekouta, Cissé, Lassana, Konaté, Mamadou, Coulibaly, Thomas, Sissoko, Adama S., Karambé, Mamadou, Burnett, Barrington, Landouré, Guida, Traoré, Moussa
Vydáno 2016Text -
7
A monoallelic variant in EYA1 is associated with Branchio‐Otic syndrome in a Malian family Autor Yalcouyé, Abdoulaye, Traoré, Oumou, Diarra, Salimata, Schrauwen, Isabelle, Esoh, Kevin, Kadlubowska, Magda Kamila, Bharadwaj, Thashi, Adadey, Samuel Mawuli, Kéita, Mohamed, Guinto, Cheick O., Leal, Suzanne M., Landouré, Guida, Wonkam, Ambroise
Vydáno 2022Text -
8
Neuropsychiatric and socio-cultural aspects in a Malian family with spinocerebellar ataxia Autor Coulibaly, Souleymane P., Coulibaly, Souleymane, Sango, Hammadoun A, Cissé, Lassana, Maïga, Fatoumata I., Maïga, Boubacar, Diarra, Salimata, Diallo, Seybou H., Coulibaly, Thomas, Traoré, Mahamadou, Guinto, Cheick O., Koumaré, Baba, Landouré, Guida
Vydáno 2019Text -
9
A novel mutation in KIF5A in a Malian family with spastic paraplegia and sensory loss Autor Guinto, Cheick O., Diarra, Salimata, Diallo, Salimata, Cissé, Lassana, Coulibaly, Thomas, Diallo, Seybou H., Taméga, Abdoulaye, Chen, Ke‐Lian, Schindler, Alice B., Bagayoko, Koumba, Simaga, Assiatou, Blackstone, Craig, Fischbeck, Kenneth H., Landouré, Guida
Vydáno 2017Text -
10
Novel mutation in the ATM gene in a Malian family with ataxia telangiectasia Autor Landouré, Guida, Mochel, Fanny, Meilleur, Katherine, Ly, Madani, Sangaré, Modibo, Bocoum, Nouhoum, Bagayoko, Koumba, Coulibaly, Thomas, Sarr, Amadou M., Bâ, Hamidou O., Coulibaly, Souleymane, Guinto, Cheick O., Touré, Mahamadou, Traoré, Moussa, Fischbeck, Kenneth H.
Vydáno 2012Text -
11
Friedreich ataxia in a family from Mali, West Africa/Friedreich ataxia in a Malian family Autor Cissé, Cheick A. K., Cissé, Lassana, Ba, Hamidou O., Samassékou, Oumar, Simaga, Assiatou, Taméga, Abdoulaye, Diarra, Salimata, Diallo, Seybou H., Coulibaly, Thomas, Diallo, Salimata, Yalcouyé, Abdoulaye, Maiga, Alassane B., Keita, Mohamed, Fischbeck, Kenneth H., Traoré, Sékou F., Guinto, Cheick O., Landouré, Guida
Vydáno 2021Text