Le informazioni sugli articoli di fonte ISI sono coperte da copyright

Per ulteriori informazioni selezionare i riferimenti di interesse.

1. Castelnau, P; Zilbovicius, M; Ribeiro, MJ; Hertz-Pannier, L; Ogier, H; Evrard, P
   Striatal and pontocerebellar hypoperfusion in Hallervorden-Spatz syndrome
   PEDIATRIC NEUROLOGY
   
   P. Castelnau et al., "Striatal and pontocerebellar hypoperfusion in Hallervorden-Spatz syndrome", PED NEUROL, 25(2), 2001, pp. 170-174
2. Sfaello, I; Castelnau, P; Blanc, N; Ogier, H; Evrard, P; Arzimanoglou, A
   Infantile spasms and Menkes disease
   EPILEPTIC DISORDERS
   
   I. Sfaello et al., "Infantile spasms and Menkes disease", EPILEPT DIS, 2(4), 2000, pp. 227-230
3. Castelnau, P; Le Merrer, M; Diatloff-Zito, C; Marquis, E; Tete, MJ; Robert, JJ
   Wolcott-Rallison syndrome: a case with endocrine and exocrine pancreatic deficiency and pancreatic hypotrophy
   EUROPEAN JOURNAL OF PEDIATRICS
   
   P. Castelnau et al., "Wolcott-Rallison syndrome: a case with endocrine and exocrine pancreatic deficiency and pancreatic hypotrophy", EUR J PED, 159(8), 2000, pp. 631-633
4. Saudubray, JM; De Lonlay, P; Touati, G; Martin, D; Nassogne, MC; Castelnau, P; Sevin, C; Laborde, C; Baussan, C; Brivet, M; Vassault, A; Rabier, D; Bonnefont, JP; Kamoun, P
   Genetic hypoglycaemia in infancy and childhood: Pathophysiology and diagnosis
   JOURNAL OF INHERITED METABOLIC DISEASE
   
   J.M. Saudubray et al., "Genetic hypoglycaemia in infancy and childhood: Pathophysiology and diagnosis", J INH MET D, 23(3), 2000, pp. 197-214
5. de Baulny, HO; Husson, I; Castelnau, P; Saudubray, JM
   Diagnosing states of ketosis in pediatrics
   ARCHIVES DE PEDIATRIE
   
   H.O. de Baulny et al., "Diagnosing states of ketosis in pediatrics", ARCH PED, 6, 1999, pp. 500S-501S
6. Gendrot, C; Ronce, N; Raynaud, M; Ayrault, AD; Dourlens, J; Castelnau, P; Muh, JP; Chelly, J; Moraine, C
   X-linked nonspecific mental retardation (MRX16) mapping to distal Xq28: Linkage study and neuropsychological data in a large family
   AMERICAN JOURNAL OF MEDICAL GENETICS
   
   C. Gendrot et al., "X-linked nonspecific mental retardation (MRX16) mapping to distal Xq28: Linkage study and neuropsychological data in a large family", AM J MED G, 83(5), 1999, pp. 411-418
7. de Lonlay, P; Cuer, M; Vuillaumier-Barrot, S; Beaune, G; Castelnau, P; Kretz, M; Durand, G; Saudubray, JM; Seta, N
   Hypersulinemic hypoglycemia as a presenting sign in phosphomannose isomerase deficiency: A new manifestation of carbohydrate-deficient glycoprotein syndrome treatable with mannose
   JOURNAL OF PEDIATRICS
   
   P. de Lonlay et al., "Hypersulinemic hypoglycemia as a presenting sign in phosphomannose isomerase deficiency: A new manifestation of carbohydrate-deficient glycoprotein syndrome treatable with mannose", J PEDIAT, 135(3), 1999, pp. 379-383
8. LAZARINI F; CASTELNAU P; CHERMANN JF; DESLYS JP; DORMONT D
   MODULATION OF PRION PROTEIN GENE-EXPRESSION BY GROWTH-FACTORS IN CULTURED MOUSE ASTROCYTES AND PC-12 CELLS
   Molecular brain research
   
   F. Lazarini et al., "MODULATION OF PRION PROTEIN GENE-EXPRESSION BY GROWTH-FACTORS IN CULTURED MOUSE ASTROCYTES AND PC-12 CELLS", Molecular brain research, 22(1-4), 1994, pp. 268-274
9. CASTELNAU P; LAZARINI F; DESLYS JP; DORMONT D
   PRION PROTEIN GENE-EXPRESSION IN CULTURED ASTROCYTES TREATED BY RECOMBINANT GROWTH-HORMONE AND INSULIN-LIKE GROWTH-FACTOR
   Experimental neurology
   
   P. Castelnau et al., "PRION PROTEIN GENE-EXPRESSION IN CULTURED ASTROCYTES TREATED BY RECOMBINANT GROWTH-HORMONE AND INSULIN-LIKE GROWTH-FACTOR", Experimental neurology, 130(2), 1994, pp. 407-410