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Journal of Medical Genetics
|
August 1, 1997
Assessment of French patients with LPL deficiency for French Canadian mutations
L Foubert, J L De Gennes, J P Lagarde, et al.
Bulletin Du Cancer
|
January 1, 1990
[Pure ovarian dysgerminoma. Evaluation of experiences and definition of a therapeutic strategy]
J M Dilhuydy, P Lagarde, J Chauvergne, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 10, 2001
Activating mutations of the calcium-sensing receptor: management of hypocalcemia
A Lienhardt, M Bai, J P Lagarde, et al.
Revue De Laryngologie - Otologie - Rhinologie
|
June 18, 1999
[Elements of epidemiology and initiation of carcinogenesis in carcinomas of the upper aerodigestive tract. Future therapeutic consequence?]
G Dolivet, P Colosetti, J L Merlin, et al.
Atherosclerosis
|
January 16, 1998
Familial defective apolipoprotein B-100 in hypercholesterolemic Chinese Canadians: identification of a unique haplotype of the apolipoprotein B-100 allele
L O Abdel-Wareth, S N Pimstone, J P Lagarde, et al.
British Journal of Cancer
|
November 1, 1992
Prognostic variables for the selection of patients with operable soft tissue sarcomas to be considered in adjuvant chemotherapy trials
A Ravaud, N B Bui, J M Coindre, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 22, 2000
A new compound heterozygous mutation of the gonadotropin-releasing hormone receptor (L314X, Q106R) in a woman with complete hypogonadotropic hypogonadism: chronic estrogen administration amplifies the gonadotropin defect
M L Kottler, S Chauvin, N Lahlou, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 19, 2000
A large homozygous or heterozygous in-frame deletion within the calcium-sensing receptor's carboxylterminal cytoplasmic tail that causes autosomal dominant hypocalcemia
A Lienhardt, M Garabédian, M Bai, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
January 1, 1992
Results of postoperative radiation therapy in medullary carcinoma of the thyroid: a retrospective study by the French Federation of Cancer Institutes--the Radiotherapy Cooperative Group
T D Nguyen, J L Chassard, P Lagarde, et al.
Vision Research
|
April 22, 1999
Exclusion of the apoE gene in autosomal dominant retinitis pigmentosa
E H Souied, P Benlian, J M Rozet, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 78) with videos related to
Sort By:
Page
of 8
Journal of Medical Genetics
|
August 1, 1997
Assessment of French patients with LPL deficiency for French Canadian mutations
L Foubert, J L De Gennes, J P Lagarde, et al.
Bulletin Du Cancer
|
January 1, 1990
[Pure ovarian dysgerminoma. Evaluation of experiences and definition of a therapeutic strategy]
J M Dilhuydy, P Lagarde, J Chauvergne, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 10, 2001
Activating mutations of the calcium-sensing receptor: management of hypocalcemia
A Lienhardt, M Bai, J P Lagarde, et al.
Revue De Laryngologie - Otologie - Rhinologie
|
June 18, 1999
[Elements of epidemiology and initiation of carcinogenesis in carcinomas of the upper aerodigestive tract. Future therapeutic consequence?]
G Dolivet, P Colosetti, J L Merlin, et al.
Atherosclerosis
|
January 16, 1998
Familial defective apolipoprotein B-100 in hypercholesterolemic Chinese Canadians: identification of a unique haplotype of the apolipoprotein B-100 allele
L O Abdel-Wareth, S N Pimstone, J P Lagarde, et al.
British Journal of Cancer
|
November 1, 1992
Prognostic variables for the selection of patients with operable soft tissue sarcomas to be considered in adjuvant chemotherapy trials
A Ravaud, N B Bui, J M Coindre, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 22, 2000
A new compound heterozygous mutation of the gonadotropin-releasing hormone receptor (L314X, Q106R) in a woman with complete hypogonadotropic hypogonadism: chronic estrogen administration amplifies the gonadotropin defect
M L Kottler, S Chauvin, N Lahlou, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 19, 2000
A large homozygous or heterozygous in-frame deletion within the calcium-sensing receptor's carboxylterminal cytoplasmic tail that causes autosomal dominant hypocalcemia
A Lienhardt, M Garabédian, M Bai, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
January 1, 1992
Results of postoperative radiation therapy in medullary carcinoma of the thyroid: a retrospective study by the French Federation of Cancer Institutes--the Radiotherapy Cooperative Group
T D Nguyen, J L Chassard, P Lagarde, et al.
Vision Research
|
April 22, 1999
Exclusion of the apoE gene in autosomal dominant retinitis pigmentosa
E H Souied, P Benlian, J M Rozet, et al.
Page
of 8