P. Dussoix

发表

Abnormal Regulation of Hepatic Glucose Output in Maturity-Onset Diabetes of the Young Caused by a Specific Mutation of the Glucokinase Gene

E. Jéquier, L. Tappy, P. Schneiter, 1997, Diabetes.

The (Ala-Val) mutation of methylenetetrahydrofolate reductase as a genetic risk factor for vascular disease in non-insulin-dependent diabetic patients.

P. Froguel, P. Passa, R. James, 1997, American journal of human genetics.

Glucose utilization and production in patients with maturity-onset diabetes of the young caused by a mutation of the hepatocyte nuclear factor-1alpha gene.

E. Guenat, P. Froguel, M. Vaxillaire, 1998, Diabetes.

Insulin, but not glucose lowering corrects the hyperglucagonemia and increased proglucagon messenger ribonucleic acid levels observed in insulinopenic diabetes.

P. Meda, A. Ktorza, M. Gilbert, 1998, Endocrinology.

Time savings with prehospital thrombolysis in an urban area

J. Gaspoz, P. Unger, P. Dussoix, 2003, European journal of emergency medicine : official journal of the European Society for Emergency Medicine.

Unusual association: Streptococcus bovis tricuspid endocarditis with atrial-septal aneurysm and patent foramen ovale.

J. Garbino, P. Dussoix, R. Sommer, 2000, Schweizerische medizinische Wochenschrift.

Penicilliosis marneffei infection in AIDS.

J. Saurat, L. Borradori, J. Schmit, 1994, Journal of the American Academy of Dermatology.

A new screening tool for SARS-CoV-2 infection based on self-reported patient clinical characteristics: the COV19-ID score

O. Kherad, M. Ramlawi, P. Dussoix, 2022, BMC Infectious Diseases.

Paraoxonase polymorphism Met-Leu54 is associated with modified serum concentrations of the enzyme. A possible link between the paraoxonase gene and increased risk of cardiovascular disease in diabetes.

P. Froguel, H. Blanché, P. Passa, 1997, The Journal of clinical investigation.

An unusual case of syncope.

P. Dussoix, T. Hagelberg, B. Vermeulen, 2004, European journal of emergency medicine : official journal of the European Society for Emergency Medicine.

Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3).

G. Lathrop, R. Cox, G. Charpentier, 1997, Human molecular genetics.

[Facial palsy: diagnosis and management by primary care physicians].

J. Gaspoz, P. Dussoix, V. Alvarez, 2009, Revue medicale suisse.

Insulin, but not glucose lowering corrects the hyperglucagonemia and increased proglucagon messenger ribonucleic acid levels observed in insulinopenic diabetes.

P. Dussoix, B. Ritz-Laser, A. Ktorza, 1998, Endocrinology.

Diagnostic Heterogeneity of Diabetes in Lean Young Adults: Classification Based on Immunological and Genetic Parameters

P. Froguel, M. Vaxillaire, G. Spinas, 1997, Diabetes.