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F Bernardi

Showing results (181-190 of 402) with videos related to

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Thrombosis and Haemostasis|February 24, 2001
Functional properties of factor V and factor Va encoded by the R2-geneL Hoekema, E Castoldi, G Tans, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1975
Relationships among the secretion of ACTH, GH, and cortisol during the insulin-induced hypoglycemia test in the normal and obese childE Cacciari, A Cicognani, P Pirazzoli, et al.
Human Molecular Genetics|July 1, 1993
A new disease-causing mutation in the GAP-related domain of the NF1 geneF Anglani, A Murgia, S Bedin, et al.
Archives of Disease in Childhood|May 1, 1981
Disordered prolactin secretion in the obese child and adolescentE Cacciari, E Frejaville, A Balsamo, et al.
Minerva Pediatrica|July 28, 1974
[Problems and results in the diagnosis and therapy of hyposomia with growth hormone deficiency]E Cacciari, A Cicognani, P Tassoni, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 26, 2011
Novel phenotype and γ-glutamyl carboxylase mutations in combined deficiency of vitamin K-dependent coagulation factorsB Lunghi, R Redaelli, T M Caimi, et al.
La Radiologia Medica|November 1, 1993
[Diagnosis of gastro-esophageal reflux in children. Ultrasonography versus pH monitoring]G Tani, R Sciutti, F Teglia, et al.
American Journal of Ophthalmology|August 24, 1999
Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotypeC Incorvaia, G Lamberti, F Parmeggiani, et al.
Human Genetics|April 1, 1988
A HindIII RFLP and a gene lesion in the coagulation factor VIII geneF Bernardi, C Legnani, S Volinia, et al.
Human Molecular Genetics|December 1, 1993
Deletion breakpoints in a 32 bp perfect repeat located 45.1 Kb apart in the human growth hormone gene clusterC Baroncini, L Baldazzi, P Pirazzoli, et al.
Pageof 41

Showing results (181-190 of 402) with videos related to

Sort By:
Pageof 41
Thrombosis and Haemostasis|February 24, 2001
Functional properties of factor V and factor Va encoded by the R2-geneL Hoekema, E Castoldi, G Tans, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 1975
Relationships among the secretion of ACTH, GH, and cortisol during the insulin-induced hypoglycemia test in the normal and obese childE Cacciari, A Cicognani, P Pirazzoli, et al.
Human Molecular Genetics|July 1, 1993
A new disease-causing mutation in the GAP-related domain of the NF1 geneF Anglani, A Murgia, S Bedin, et al.
Archives of Disease in Childhood|May 1, 1981
Disordered prolactin secretion in the obese child and adolescentE Cacciari, E Frejaville, A Balsamo, et al.
Minerva Pediatrica|July 28, 1974
[Problems and results in the diagnosis and therapy of hyposomia with growth hormone deficiency]E Cacciari, A Cicognani, P Tassoni, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 26, 2011
Novel phenotype and γ-glutamyl carboxylase mutations in combined deficiency of vitamin K-dependent coagulation factorsB Lunghi, R Redaelli, T M Caimi, et al.
La Radiologia Medica|November 1, 1993
[Diagnosis of gastro-esophageal reflux in children. Ultrasonography versus pH monitoring]G Tani, R Sciutti, F Teglia, et al.
American Journal of Ophthalmology|August 24, 1999
Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotypeC Incorvaia, G Lamberti, F Parmeggiani, et al.
Human Genetics|April 1, 1988
A HindIII RFLP and a gene lesion in the coagulation factor VIII geneF Bernardi, C Legnani, S Volinia, et al.
Human Molecular Genetics|December 1, 1993
Deletion breakpoints in a 32 bp perfect repeat located 45.1 Kb apart in the human growth hormone gene clusterC Baroncini, L Baldazzi, P Pirazzoli, et al.
Pageof 41