P. Bouloux

发表

Mirror movements in X-linked Kallmann's syndrome. I. A neurophysiological study.

L. Harrison, J. Stephens, M. Krams, 1997, Brain : a journal of neurology.

Proteinuria, hypertension and chronic renal failure in X-linked Kallmann's syndrome, a defined genetic cause of solitary functioning kidney.

R. Quinton, P. Bouloux, A. Woolf, 1998, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Coding sequence analysis of GNRHR and GPR54 in patients with congenital and adult-onset forms of hypogonadotropic hypogonadism.

P. Bouloux, Felecia Cerrato, C. Welt, 2006, European journal of endocrinology.

KAL, a gene mutated in Kallmann's syndrome, is expressed in the first trimester of human development

P. Bouloux, A. Woolf, P. Winyard, 1995, Molecular and Cellular Endocrinology.

Treatment of male infertility

R. Quinton, P. Bouloux, V. Duke, 1994, The Lancet.

Ghrelin Can Bind to a Species of High Density Lipoprotein Associated with Paraoxonase*

P. Bouloux, M. Vanderpump, V. Skinner, 2003, The Journal of Biological Chemistry.

Kallmann’s syndrome

Karl J. Friston, K J Friston, J Ashburner, 1999, Neurology.

Growth hormone therapy for non-islet cell tumor hypoglycemia.

P. Bouloux, L. Silveira, F. Miraki-Moud, 2002, The American journal of medicine.

An unusual steroid-producing ovarian tumour: case report.

P. Bouloux, A. Maclean, J. Stephens, 2002, Human reproduction.

Comparison of serum FSH and Inhibin B levels between adult male dizygotic and monozygotic twins.

T. Spector, P. Sambrook, P. Bouloux, 2006, Human reproduction.

Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes

E. Fliers, R. Quinton, P. Bouloux, 2006, Molecular and Cellular Endocrinology.

Successful induction of fertility in a hypogonadotropic male

R. Quinton, P. Bouloux, G. Matfin, 1994, The Lancet.

Identification of olfactory dysfunction in carriers of X‐linked Kallmann's syndrome

R. Quinton, P. Bouloux, J. Kirk, 1995 .

Identification of olfactory dysfunction in carriers of X‐linked Kallmann's syndrome

P. Bouloux, G. Besser, J. Kirk, 1994, Clinical endocrinology.

Unilateral renal aplasia in X‐linked Kallmann's syndrome

R. Quinton, P. Bouloux, O. Edwards, 1994, Clinical genetics.

GnRH neuronal development: insights into hypogonadotrophic hypogonadism

R. Quinton, P. Bouloux, G. Maccoll, 2002, Trends in Endocrinology & Metabolism.

Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism.

Shaun K Olsen, Taneli Raivio, Richard Quinton, 2007, The Journal of clinical investigation.

Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations

M. Hauschild, P. Bouloux, M. Polak, 2014, Genetics in Medicine.

Multicystic dysplastic kidney and Kallmann's syndrome: a new association?

P. Bouloux, N. Moghal, A. Woolf, 2001, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Hypogonadotropic Hypogonadism

P. Bouloux, L. Silveira, G. Maccoll, 2002, Seminars in reproductive medicine.

Mirror movements in X-linked Kallmann's syndrome. II. A PET study.

R. Dolan, R. Passingham, R. Frackowiak, 1997, Brain : a journal of neurology.

Kallmann Syndrome Adhesion, Afferents, and Anosmia

R. Quinton, P. Bouloux, G. Maccoll, 2002, Neuron.

Routine neuroimaging in classical isolated gonadotrophin deficiency is of limited clinical value

R. Quinton, P. Bouloux, G. Conway, 2001, Clinical endocrinology.

The sweating apparatus in growth hormone deficiency, following treatment with r-hGH and in acromegaly

P. Bouloux, T. Cowen, W. Hasan, 2001, Autonomic Neuroscience.

Molecular Genetics and Neurobiology of Kallmann’s Syndrome

R. Quinton, P. Bouloux, V. Duke, 1996 .