ACNP - Italian Periodicals Catalogue

AAAAAA

ITA
ENG

Results: 1-12 |

Results: 12

CONGENITAL INSENSITIVITY TO PAIN WITH ANHYDROSIS - REPORT OF 2 UNRELATED CASES

Authors: VITAL A FONTAN D JULIEN J TALON P HERON B ROUTON MC PONSOT G VITAL C

Citation: A. Vital et al., CONGENITAL INSENSITIVITY TO PAIN WITH ANHYDROSIS - REPORT OF 2 UNRELATED CASES, Journal of the peripheral nervous system, 3(2), 1998, pp. 125-132

PERSISTENT HYPOCITRULLINAEMIA AS A MARKER FOR MTDNA NARP T-8993 G-MUTATION

Authors: RABIER D DIRY C ROTIG A RUSTIN P HERON B BARDET J PARVY P PONSOT G MARSAC C SAUDUBRAY JM MUNNICH A KAMOUN P

Citation: D. Rabier et al., PERSISTENT HYPOCITRULLINAEMIA AS A MARKER FOR MTDNA NARP T-8993 G-MUTATION, Journal of inherited metabolic disease, 21(3), 1998, pp. 216-219

CEREBRAL INFARCTION IN PEDIATRIC-PATIENTS - A REVIEW OF 60 CASES

Authors: TABARKI B HERON B PONSOT G

Citation: B. Tabarki et al., CEREBRAL INFARCTION IN PEDIATRIC-PATIENTS - A REVIEW OF 60 CASES, Annales de pediatrie, 45(2), 1998, pp. 65-71

A NEAR HOMOPLASMIC T8993G MTDNA MUTATION IN A PATIENT WITH ATYPIC LEIGH-SYNDROME NOT PRESENT IN THE MOTHERS TISSUES

Authors: DEGOUL F FRANCOIS D DIRY M PONSOT G DESGUERRE I HERON B MARSAC C MOUTARD ML

Citation: F. Degoul et al., A NEAR HOMOPLASMIC T8993G MTDNA MUTATION IN A PATIENT WITH ATYPIC LEIGH-SYNDROME NOT PRESENT IN THE MOTHERS TISSUES, Journal of inherited metabolic disease, 20(1), 1997, pp. 49-53

HERIOT-WATT ALUMNI

Authors: HERON B

Citation: B. Heron, HERIOT-WATT ALUMNI, Chemistry in Britain, 33(11), 1997, pp. 19-19

HERIOT-WATT ALUMNI

Authors: HERON B

Citation: B. Heron, HERIOT-WATT ALUMNI, Chemistry and Industry, (9), 1997, pp. 328-328

RELAXED GAMMA-CONVERGENCE AND APPLICATION TO NONCOERCIVE PROBLEMS

Authors: GUSTAFSSON B HERON B MOSSINO J

Citation: B. Gustafsson et al., RELAXED GAMMA-CONVERGENCE AND APPLICATION TO NONCOERCIVE PROBLEMS, Comptes rendus de l'Academie des sciences. Serie 1, Mathematique, 323(1), 1996, pp. 7-12

ACUTE APPENDICITIS IN INFANTS

Authors: HERON B ALLAS F FAYAD F CHALVON A NATHANSON M GAUDELUS J

Citation: B. Heron et al., ACUTE APPENDICITIS IN INFANTS, La Presse medicale, 24(15), 1995, pp. 736-736

ESTABLISHMENT OF HUMAN MICROGLIAL CELL-LINES AFTER TRANSFECTION OF PRIMARY CULTURES OF EMBRYONIC MICROGLIAL CELLS WITH THE SV40 LARGE T-ANTIGEN

Authors: JANABI N PEUDENIER S HERON B NG KH TARDIEU M

Citation: N. Janabi et al., ESTABLISHMENT OF HUMAN MICROGLIAL CELL-LINES AFTER TRANSFECTION OF PRIMARY CULTURES OF EMBRYONIC MICROGLIAL CELLS WITH THE SV40 LARGE T-ANTIGEN, Neuroscience letters, 195(2), 1995, pp. 105-108

DIAGNOSIS OF COMA OF METABOLIC ORIGIN IN CHILDREN

Authors: POGGITRAVERT F HERON B DEVILLEMEUR TB SPADA M JOUVET P CHARPENTIER C RABIER D KAMOUN P SAUDUBRAY JM

Citation: F. Poggitravert et al., DIAGNOSIS OF COMA OF METABOLIC ORIGIN IN CHILDREN, Archives de pediatrie, 1(9), 1994, pp. 843-851

LET US GO ON WITH VITAMIN-D SUPPLEMENTATI ON

Authors: DEMERSAY AC BENHAJYEDDER A HERON B NATHANSON M GAUDELUS J

Citation: Ac. Demersay et al., LET US GO ON WITH VITAMIN-D SUPPLEMENTATI ON, Archives de pediatrie, 1(9), 1994, pp. 855-856

BIOTINIDASE DEFICIENCY - A BIOTIN-RESPONS IVE ENCEPHALOPATHY WITH EPILEPSY

Authors: HERON B GAUTIER A DULAC O PONSOT G

Citation: B. Heron et al., BIOTINIDASE DEFICIENCY - A BIOTIN-RESPONS IVE ENCEPHALOPATHY WITH EPILEPSY, Archives francaises de pediatrie, 50(10), 1993, pp. 875-878

Risultati: 1-12 |