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Human Genetics
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July 1, 1992
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine alpha 1(I) 901 substitution in a type-I collagen gene
M Mottes, A Sangalli, M Valli, et al.
European Journal of Gynaecological Oncology
|
January 1, 1987
Surgical strategy management following lymph nodal positivity at the three levels (a retrospective and perspective study)
M Valli, A Lanza, R Giani, et al.
Therapie
|
March 10, 2001
[Accidental ingestion of paracetamol in the for of the pediatric syrup EFFERALGAN: case studies during the six months following the institution of the child-proof top]
L de Haro, L Tichadou, N Prost, et al.
Presse Medicale (Paris, France : 1983)
|
January 5, 2002
[Lead poisoning in adults. Experience of the Poison Control Center of Marseille from 1993 to 2000]
L de Haro, N Prost, D Gambini, et al.
Therapie
|
August 21, 2002
[Is nitroxoline an allergen?]
F Rodor, M Castelain, N Prost, et al.
Human Mutation
|
January 1, 1993
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta
M Mottes, M M Gomez Lira, M Valli, et al.
L'Encephale
|
January 1, 1990
[Plasma levels of metapramine and its 3 major metabolites in patients with depression. Results and preliminary interpretations]
T Bougerol, F Gouezo, P Pok Phak Rop, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
July 29, 1998
Interphysician variability in defining the planning target volume in the irradiation of prostate and seminal vesicles
L F Cazzaniga, M A Marinoni, A Bossi, et al.
L'Encephale
|
November 1, 1985
[Multidisciplinary approach to depression. Preliminary results]
R Arnaud-Castiglioni, T Bougerol, H Chakroun, et al.
The Journal of Biological Chemistry
|
January 25, 1991
A de novo G to T transversion in a pro-alpha 1 (I) collagen gene for a moderate case of osteogenesis imperfecta. Substitution of cysteine for glycine 178 in the triple helical domain
M Valli, M Mottes, R Tenni, et al.
Page
of 18
Search research articles
Search
Showing results (161-170 of 177) with videos related to
Sort By:
Page
of 18
Human Genetics
|
July 1, 1992
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine alpha 1(I) 901 substitution in a type-I collagen gene
M Mottes, A Sangalli, M Valli, et al.
European Journal of Gynaecological Oncology
|
January 1, 1987
Surgical strategy management following lymph nodal positivity at the three levels (a retrospective and perspective study)
M Valli, A Lanza, R Giani, et al.
Therapie
|
March 10, 2001
[Accidental ingestion of paracetamol in the for of the pediatric syrup EFFERALGAN: case studies during the six months following the institution of the child-proof top]
L de Haro, L Tichadou, N Prost, et al.
Presse Medicale (Paris, France : 1983)
|
January 5, 2002
[Lead poisoning in adults. Experience of the Poison Control Center of Marseille from 1993 to 2000]
L de Haro, N Prost, D Gambini, et al.
Therapie
|
August 21, 2002
[Is nitroxoline an allergen?]
F Rodor, M Castelain, N Prost, et al.
Human Mutation
|
January 1, 1993
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta
M Mottes, M M Gomez Lira, M Valli, et al.
L'Encephale
|
January 1, 1990
[Plasma levels of metapramine and its 3 major metabolites in patients with depression. Results and preliminary interpretations]
T Bougerol, F Gouezo, P Pok Phak Rop, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
July 29, 1998
Interphysician variability in defining the planning target volume in the irradiation of prostate and seminal vesicles
L F Cazzaniga, M A Marinoni, A Bossi, et al.
L'Encephale
|
November 1, 1985
[Multidisciplinary approach to depression. Preliminary results]
R Arnaud-Castiglioni, T Bougerol, H Chakroun, et al.
The Journal of Biological Chemistry
|
January 25, 1991
A de novo G to T transversion in a pro-alpha 1 (I) collagen gene for a moderate case of osteogenesis imperfecta. Substitution of cysteine for glycine 178 in the triple helical domain
M Valli, M Mottes, R Tenni, et al.
Page
of 18