P. Cochaux

P. Vereerstraeten, D. Abramowicz, M. Abramowicz, 2010, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Standardization of molecular monitoring of CML: results and recommendations from the European treatment and outcome study

D. Colomer, J. Cayuela, S. Balabanov, 2022, Leukemia.

Pathogenesis of autonomous thyroid nodules: in vitro study of iodine and adenosine 3',5'-monophosphate metabolism.

P. Rocmans, J. Mockel, J. Dumont, 1988, The Journal of clinical endocrinology and metabolism.

Effects of prostaglandins F alpha on dog thyroid cyclic AMP level and function.

J. Dumont, J. Boeynaems, J. van Sande, 1982, Biochimica et biophysica acta.

The deltaccr5 mutation conferring protection against HIV-1 in Caucasian populations has a single and recent origin in Northeastern Europe.

L. Peltonen, M. Parmentier, A. Czeizel, 1998, Human molecular genetics.

IODIDE ORGANIFICATION DEFECT IN A COLD THYROID NODULE: ABSENCE OF IODIDE EFFECT ON CYCLIC AMP ACCUMULATION

J. Dumont, J. Sande, P. Cochaux, 1984, Clinical endocrinology.

Disseminated angiosarcoma presenting as a hemophagocytic syndrome in a renal allograft recipient

P. Vereerstraeten, D. Abramowicz, C. Wolf‐peeters, 1997, Transplant international : official journal of the European Society for Organ Transplantation.

Further characterization of the iodide inhibitory effect on the cyclic AMP system in dog thyroid slices

J. Dumont, J. Sande, P. Cochaux, 1985, Molecular and Cellular Endocrinology.

Systemic responsiveness to lipopolysaccharide and polymorphisms in the toll-like receptor 4 gene in human beings.

R. Rylander, P. Holt, M. Dentener, 2003, The Journal of allergy and clinical immunology.

Identification of a minor Tg mRNA transcript in RNA from normal and goitrous thyroids

D. Corach, G. Vassart, H. Targovnik, 1992, Molecular and Cellular Endocrinology.

Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas

J. Parma, J. Mockel, J. Dumont, 1993, Nature.

Brief report: clonal proliferation of type 2 helper T cells in a man with the hypereosinophilic syndrome.

M. Goldman, T. Velu, A. Crusiaux, 1994, The New England journal of medicine.

DNA fingerprinting in man using a mouse probe related to part of the Drosophila 'Per' gene.

M. Georges, G. Vassart, P. Cochaux, 1987, Nucleic acids research.

TCF7L2 polymorphism associates with new-onset diabetes after transplantation.

D. Abramowicz, M. Abramowicz, K. Wissing, 2009, Journal of the American Society of Nephrology : JASN.

Experience with 1251 transcervical chorionic villus samplings performed in the first trimester by a single team of operators.

M. Abramowicz, C. Donner, F. Rodesch, 1995, European journal of obstetrics, gynecology, and reproductive biology.

Pernicious anaemia and hypoparathyroidism in a patient with Kearns-Sayre syndrome with mitochondrial DNA duplication

M. Abramowicz, E. Vamos, P. Cochaux, 1996, Journal of Inherited Metabolic Disease.

Proximal deletion of chromosome 21 confirmed by in situ hybridization and molecular studies.

F. Speleman, N. Van Roy, N. van Regemorter, 1994, American journal of medical genetics.

Relative contribution of Ki-ras gene analysis and brush cytology during ERCP for the diagnosis of biliary and pancreatic diseases.

J. Parma, J. Devière, V. Bourgeois, 1998, Gastrointestinal endoscopy.

A nonsense mutation causes human hereditary congenital goiter with preferential production of a 171-nucleotide-deleted thyroglobulin ribonucleic acid messenger.

G. Vassart, H. Targovnik, G. Medeiros-Neto, 1993, The Journal of clinical endocrinology and metabolism.

Islet‐activating protein discriminates between different inhibitors of thyroidal cyclic AMP system

J. van Sande, P. Cochaux, J. Dumont, 1985, FEBS letters.

Induction of specific T‐cell responses in HIV infection

E. Sandström, B. Wahrén, G. Bratt, 1998, AIDS.

Clinical and genetical manifestations in 34 families with Leber's hereditary optic neuropathy (LHON).

C. Broux, P. Cochaux, C. Candaele, 1994, Bulletin de la Societe belge d'ophtalmologie.

Neonatal haemoglobinopathy screening: review of a 10-year programme in Brussels

F. Vertongen, F. Cotton, B. Gulbis, 2006, Journal of medical screening.

Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.

T. Meitinger, B. Lorenz, K. Zerres, 1994, American journal of human genetics.

[Medical genetics service].

J. Parma, M. Abramowicz, G. Vassart, 2002, Revue medicale de Bruxelles.

Thyroid control: an example of a complex cell regulation network.

J. Mockel, J. Dumont, F. Lamy, 1981, Advances in cyclic nucleotide research.

Negative regulation of cyclic AMP levels by activation of cyclic nucleotide phosphodiesterases: the example of the dog thyroid.

J. Dumont, F. Miot, C. Erneux, 1984, Advances in cyclic nucleotide and protein phosphorylation research.

Rapid and easy prenatal diagnosis of sickle cell anemia using double‐dye LNA probe technology

J. Vandesompele, J. Parma, P. Vannuffel, 2007, British journal of haematology.

[Sickle cell disease: exotic disease or a Belgian public health problem?].

A. Kentos, F. Vertongen, F. Cotton, 2005, Revue medicale de Bruxelles.