Nougues, P.
38  Ergebnisse:
Personensuche X
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2

We know where you are going: tracking objects in terrain:

Nougues, P.
IMA Journal of Management Mathematics.  8 (1997)  1 - p. 39-58 , 1997
 
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4

9 cantiques pour la messe basse du dimanche : ou paraphrase..:

Nougues, P. (Abbé)
http://catalogues.toulouse.fr/web2/tramp2.exe/do_keyword_search/log_in?setting_key=BMT1&servers=1home&query=RMB_000418.  , 1800
 
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5

COLLAGEN RELATED MUSCLE DISEASES:

Metay, C. ; Jobic, V. ; Isapof, A....
Neuromuscular Disorders.  31 (2021)  - p. S67 , 2021
 
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7

P299 – 1889 Congenital myasthenic syndromes: classification..:

Echenne, B ; Sternberg, D ; Richard, P...
European Journal of Paediatric Neurology.  17 (2013)  - p. S136 , 2013
 
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9

Polyhandicap and aging:

Rousseau, Marie-Christine ; de Villemeur, Thierry Billette ; Khaldi-Cherif, Sherezad...
Disability and Health Journal.  12 (2019)  4 - p. 657-664 , 2019
 
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10

¿Pocos legisladores buenos hacen más que muchos malos? El r..:

J. J. Bercoff y J. P. Nougués
https://revistas.ort.edu.uy/letras-internacionales/article/view/677/675.  , 2012
 
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11

An attempt to correlate early muscle characteristics with c..:

Vigneron, P ; Nougues, J ; Bacou, F..
Livestock Production Science.  11 (1984)  2 - p. 195-205 , 1984
 
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12

HIDEA syndrome is caused by biallelic, pathogenic, rare or ..:

Kraatari-Tiri, M ; Soikkonen, L ; Myllykoski, M...
https://openaccess.sgul.ac.uk/id/eprint/114645/6/Clinical%20Genetics%20-%202022%20-%20Kraatari%E2%80%90Tiri%20-%20HIDEA%20syndrome%20is%20caused%20by%20biallelic%20pathogenic%20rare%20or%20founder%20P4HTM.pdf.  , 2022
 
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13

KCNT1-related epilepsies and epileptic encephalopathies:phe..:

Bonardi, Claudia M ; Heyne, Henrike O ; Fiannacca, Martina...
Bonardi , C M , Heyne , H O , Fiannacca , M , Fitzgerald , M P , Gardella , E , Gunning , B , Olofsson , K , Lesca , G , Verbeek , N , Stamberger , H , Striano , P , Zara , F , Mancardi , M M , Nava , C , Syrbe , S , Buono , S , Baulac , S , Coppola , A , Weckhuysen , S , Schoonjans , A-S , Ceulemans , B , Sarret , C , Baumgartner , T , Muhle , H , des Portes , V , Toulouse , J , Nougues , M-C , Rossi , M , Demarquay , G , Ville , D , Hirsch , E , Maurey , H , Willems , M , de Bellescize , J , Altuzarra , C D , Villeneuve , N , Bartolomei , F , Picard , F , Hornemann , F , Koolen , D A , Kroes , H Y , Reale , C , Fenger , C D , Tan , W-H , Dibbens , L , Bearden , D R , Møller , R S & Rubboli , G 2021 , ' KCNT1-related epilepsies and epileptic encephalopathies : phenotypic and mutational spectrum ' , Brain : a journal of neurology , vol. 144 , no. 12 , pp. 3635-3650 . https://doi.org/10.1093/brain/awab219.  , 2021
 
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