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Acta Psychiatrica Belgica
|
July 1, 1986
[Life events and breast cancer. Initial results of a comparative study dealing with 100 cases and their control]
J L Terra, F Amiel-Lebigre, F Boujema, et al.
Journal De Genetique Humaine
|
September 1, 1985
[Evaluation of 100 autopsies performed in the maternity service of the Hôtel-Dieu in Lyon during an 18 month period]
M P Cordier, G Sournies, Y Domenichini, et al.
La Revue Francaise D'Endocrinologie Clinique, Nutrition, Et Metabolisme
|
May 1, 1972
[Hyperthyroidism and thyroid cancer]
P Guinet, J Tourniaire, A Radi, et al.
Gynecologic Oncology
|
December 26, 2017
Racial/ethnic differences in HPV 16/18 genotypes and integration status among women with a history of cytological abnormalities
J R Montealegre, E C Peckham-Gregory, D Marquez-Do, et al.
Journal of Hepatology
|
June 1, 1997
Woodchuck hepatitis virus-induced carcinoma as a relevant natural model for therapy of human hepatoma
C Gouillat, D Manganas, F Zoulim, et al.
Research in Virology
|
January 1, 1989
Rift Valley fever among domestic animals in the recent West African outbreak
T G Ksiazek, A Jouan, J M Meegan, et al.
Histopathology
|
December 6, 2005
Genetic heterogeneity in supratentorial and infratentorial primitive neuroectodermal tumours of the central nervous system
M M Inda, C Perot, M Guillaud-Bataille, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
February 14, 2015
Screening in asymptomatic SDHx mutation carriers: added value of ¹⁸F-FDG PET/CT at initial diagnosis and 1-year follow-up
C Lepoutre-Lussey, C Caramella, F Bidault, et al.
European Journal of Endocrinology
|
October 23, 2013
Systematic screening for PRKAR1A gene rearrangement in Carney complex: identification and functional characterization of a new in-frame deletion
M Guillaud Bataille, Y Rhayem, S B Sousa, et al.
Clinical Genetics
|
March 17, 2017
Reassessing the clinical spectrum associated with hereditary leiomyomatosis and renal cell carcinoma syndrome in French FH mutation carriers
M Muller, S Ferlicot, M Guillaud-Bataille, et al.
Page
of 7
Search research articles
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Showing results (61-70 of 70) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 70 results.
Acta Psychiatrica Belgica
|
July 1, 1986
[Life events and breast cancer. Initial results of a comparative study dealing with 100 cases and their control]
J L Terra, F Amiel-Lebigre, F Boujema, et al.
Journal De Genetique Humaine
|
September 1, 1985
[Evaluation of 100 autopsies performed in the maternity service of the Hôtel-Dieu in Lyon during an 18 month period]
M P Cordier, G Sournies, Y Domenichini, et al.
La Revue Francaise D'Endocrinologie Clinique, Nutrition, Et Metabolisme
|
May 1, 1972
[Hyperthyroidism and thyroid cancer]
P Guinet, J Tourniaire, A Radi, et al.
Gynecologic Oncology
|
December 26, 2017
Racial/ethnic differences in HPV 16/18 genotypes and integration status among women with a history of cytological abnormalities
J R Montealegre, E C Peckham-Gregory, D Marquez-Do, et al.
Journal of Hepatology
|
June 1, 1997
Woodchuck hepatitis virus-induced carcinoma as a relevant natural model for therapy of human hepatoma
C Gouillat, D Manganas, F Zoulim, et al.
Research in Virology
|
January 1, 1989
Rift Valley fever among domestic animals in the recent West African outbreak
T G Ksiazek, A Jouan, J M Meegan, et al.
Histopathology
|
December 6, 2005
Genetic heterogeneity in supratentorial and infratentorial primitive neuroectodermal tumours of the central nervous system
M M Inda, C Perot, M Guillaud-Bataille, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
February 14, 2015
Screening in asymptomatic SDHx mutation carriers: added value of ¹⁸F-FDG PET/CT at initial diagnosis and 1-year follow-up
C Lepoutre-Lussey, C Caramella, F Bidault, et al.
European Journal of Endocrinology
|
October 23, 2013
Systematic screening for PRKAR1A gene rearrangement in Carney complex: identification and functional characterization of a new in-frame deletion
M Guillaud Bataille, Y Rhayem, S B Sousa, et al.
Clinical Genetics
|
March 17, 2017
Reassessing the clinical spectrum associated with hereditary leiomyomatosis and renal cell carcinoma syndrome in French FH mutation carriers
M Muller, S Ferlicot, M Guillaud-Bataille, et al.
Page
of 7