C. Brachet

发表

Increasing knowledge in IGF1R defects: lessons from 35 new patients

Y. Le Bouc, M. Cuvelier, B. Isidor, 2019, Journal of Medical Genetics.

Endothelial and platelet microparticles in vasculitis of the young.

D. Mant, N. Klein, A. Harnden, 2004, Arthritis and rheumatism.

Pubertal induction and transition to adult sex hormone replacement in patients with congenital pituitary or gonadal reproductive hormone deficiency: an Endo-ERN clinical practice guideline

O. Dekkers, T. Raivio, S. Ahmed, 2022, European journal of endocrinology.

Central precocious puberty after interpersonal transfer of testosterone gel: just a coincidence?

C. Heinrichs, C. Brachet, 2012, Journal of pediatric endocrinology & metabolism : JPEM.

Hydroxyurea treatment for sickle cell disease: impact on haematopoietic stem cell transplantation's outcome

A. Gourdin, E. Sariban, P. Lê, 2004, Bone Marrow Transplantation.

Complex Tissue‐Specific Epigenotypes in Russell–Silver Syndrome Associated with 11p15 ICR1 Hypomethylation

I. Netchine, S. Rossignol, S. Azzi, 2014, Human mutation.

Nonsyndromic bilateral and unilateral optic nerve aplasia: first familial occurrence and potential implication of CYP26A1 and CYP26C1 genes

B. Menten, E. De Baere, C. Christophe, 2011, Molecular vision.

Association of parathyroid adenoma and familial hypocalciuric hypercalcaemia in a teenager.

W. Lissens, G. Andry, C. Heinrichs, 2009, European journal of endocrinology.

Adult Height after Growth Hormone Treatment at Pubertal Onset in Short Adolescents Born Small for Gestational Age: Results from a Belgian Registry-Based Study

Raoul Rooman, M. Roelants, G. Massa, 2018, International journal of endocrinology.

Hearing Loss Is Part of the Clinical Picture of ENPP1 Loss of Function Mutation

P. Deltenre, A. Mansbach, C. Heinrichs, 2013, Hormone Research in Paediatrics.

SRY‐negative 46,XX testicular/ovotesticular DSD: Long‐term outcomes and early blockade of gonadotropic axis

C. Bouvattier, K. McElreavey, M. Peuchmaur, 2020, Clinical endocrinology.

Long-Term Treatment of Hyponatremic Patients with Nephrogenic Syndrome of Inappropriate Antidiuresis: Personal Experience and Review of Published Case Reports

C. Heinrichs, G. Decaux, F. Vandergheynst, 2012, Nephron Clinical Practice.

Children With Sickle Cell Disease: Growth and Gonadal Function After Hematopoietic Stem Cell Transplantation

C. Heinrichs, A. Ferster, C. Devalck, 2007, Journal of pediatric hematology/oncology.

Children’s virilization and the use of a testosterone gel by their fathers

C. Heinrichs, C. Brachet, J. Vermeulen, 2005, European Journal of Pediatrics.

Nephrogenic Syndrome of Inappropriate Antidiuresis in a Female Neonate: Review of the Clinical Presentation in Females

C. Heinrichs, F. Vandergheynst, C. Brachet, 2015, Hormone Research in Paediatrics.

Growth retardation in untreated autosomal dominant familial neurohypophyseal diabetes insipidus caused by one recurring and two novel mutations in the vasopressin-neurophysin II gene.

B. Velkeniers, C. Christophe, J. Rutishauser, 2011, European journal of endocrinology.

Live birth after autograft of ovarian tissue cryopreserved during childhood.

A. Ferster, P. Simon, F. Moffa, 2015, Human reproduction.

Delayed diagnosis of congenital hypopituitarism associated with low socio-economic status and/or migration

C. Heinrichs, C. Brachet, E. Boros, 2019, European Journal of Pediatrics.

A novel approach in the intraoperative management of ovotesticular DSD.

C. Heinrichs, C. Brachet, X. Delforge, 2020, Journal of Pediatric Urology.

Contribution of functionally assessed GHRHR mutations to idiopathic isolated growth hormone deficiency in patients without GH1 mutations

P. Chanson, M. Polak, S. Lyonnet, 2019, Human mutation.

Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, a Gene Implicated in Ubiquitination

C. Rivolta, T. Langmann, P. Farinelli, 2016, American journal of human genetics.

Primary Ovarian Insufficiency in RMND1 Mitochondrial Disease.

S. Seneca, A. Aeby, C. Brachet, 2022, Mitochondrion.

Haematopoietic stem cell transplantation for severe sickle cell disease in childhood: a single centre experience of 50 patients

P. Lê, A. Ferster, C. Devalck, 2014, British journal of haematology.

Abstract presented at the 21st Annual Congress of the Belgian Society of Internal Medicine - Joint meeting with the Belgian Society of Infectiology and Clinical Microbiology

C. Libioulle, V. Bours, V. Dideberg, 2016, Acta clinica Belgica.

The Retina in Patients With Triple A Syndrome: A Window Into Neurodegeneration?

I. Balikova, C. Heinrichs, C. Vilain, 2021, Frontiers in Endocrinology.

Six Novel Variants in the MKRN3 Gene Causing Central Precocious Puberty

C. Libioulle, C. Heinrichs, S. Tenoutasse, 2022, Journal of the Endocrine Society.

Autosomal Dominant Hypocalcemia Type I: About Difficult Management Despite 1-34 Recombinant PTH Treatment in an Infant

C. Heinrichs, C. Brachet, E. Boros, 2022 .

Efficacy and safety of a 4-year combination therapy of growth hormone and gonadotropin-releasing hormone analogue in pubertal girls with short predicted adult height

Raoul Rooman, S. Verhulst, M. Cools, 2023, Frontiers in Endocrinology.

Truncating RAX Mutations: Anophthalmia, Hypopituitarism, Diabetes Insipidus, and Cleft Palate in Mice and Men.

G. Smits, I. Balikova, P. Mathers, 2019, Journal of Clinical Endocrinology and Metabolism.

Symptomatic heterozygotes and prenatal diagnoses in a nonconsanguineous family with syndromic combined pituitary hormone deficiency resulting from two novel LHX3 mutations.

S. Amselem, B. Copin, M. Legendre, 2012, The Journal of clinical endocrinology and metabolism.

[Bilateral breast masses].

M. Ost, L. Debusscher, C. Brachet, 2000, Revue Medicale de Bruxelles.

Congenital Hypothyroidism: Long-Term Experience with Early and High Levothyroxine Dosage

C. Heinrichs, G. Van Vliet, S. Tenoutasse, 2016, Hormone Research in Paediatrics.

Growth response of syndromic versus non-syndromic children born small for gestational age (SGA) to growth hormone therapy: a Belgian study

C. Heinrichs, J. De Schepper, M. Thomas, 2023, Frontiers in Endocrinology.

Live birth after autograft of ovarian tissue cryopreserved during childhood.

A. Ferster, P. Simon, F. Moffa, 2015, Human Reproduction.

Hypothyroidism due to bi-allelic variants in IYD: description of four families and a novel variant.

N. Driessens, C. Brachet, E. Boros, 2024, European journal of endocrinology.

Complex Tissue‐Specific Epigenotypes in Russell–Silver Syndrome Associated with 11p15 ICR1 Hypomethylation

I. Netchine, S. Rossignol, S. Azzi, 2014, Human mutation.