C. Heinrichs

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11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations.

G. Pinto, C. Gicquel, Y. Le Bouc, 2007, The Journal of clinical endocrinology and metabolism.

Trends in age at diagnosis of Turner syndrome

F. de Zegher, M. Craen, C. Heinrichs, 2005, Archives of Disease in Childhood.

ADULTHOOD: THE BELGIAN EXPERIENCE

G. Massa, C. Heinrichs, J. Bourguignon, 2021 .

Diagnosis of rotator cuff lesions: comparison of US and MRI on 38 joint specimens

M. Rominger, C. Heinrichs, C. Melzer, 1997, European Radiology.

Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland.

J. Parma, M. Abramowicz, G. Vassart, 1997, The Journal of clinical investigation.

PRKAR1A and PDE4D mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistance.

P. Wicart, J. Argente, P. Bougnères, 2012, The Journal of clinical endocrinology and metabolism.

Myocardial Injury and Repair

J. Schaper, S. Hein, C. Heinrichs, 1992 .

Sexual precocity after immigration from developing countries to Belgium: evidence of previous exposure to organochlorine pesticides

J. Bourguignon, C. Charlier, G. Plomteux, 2001 .

Effects of 17 months treatment using recombinant insulin‐like growth factor‐I in two children with growth hormone insensitivity (Laron) syndrome

C. Heinrichs, J. Bourguignon, P. Bergmann, 1993, Clinical endocrinology.

Ghrelin Is Suppressed by Glucagon and Does Not Mediate Glucagon-Related Growth Hormone Release

D. Cummings, C. Heinrichs, J. Chanoine, 2005, Hormone Research in Paediatrics.

Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8.

J. Parma, M. Abramowicz, S. Costagliola, 2001, The Journal of clinical endocrinology and metabolism.

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

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

Health and Psychosocial Status of Patients with Turner Syndrome after Transition to Adulthood: The Belgian Experience

M. Craen, C. Heinrichs, G. Massa, 2004, Hormone Research in Paediatrics.

Growth hormone therapy in Turner's syndrome: one versus two daily injections.

M. Craen, C. Heinrichs, G. Massa, 1994, The Journal of clinical endocrinology and metabolism.

Sexual precocity after immigration from developing countries to Belgium: evidence of previous exposure to organochlorine pesticides.

C. de Beaufort, J. Bourguignon, C. Charlier, 2001, Human reproduction.

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

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

Infant Primary Hypothyroidism as the First Manifestation of Pseudohypoparathyroidism Type 1a.

N. Perlmutter, E. Mallet, N. Loveridge, 1995 .

Prevalence and demographic features of childhood growth hormone deficiency in Belgium during the period 1986-2001.

F. de Zegher, M. Craen, C. Heinrichs, 2004, European journal of endocrinology.

Discordance of monozygotic twins for thyroid dysgenesis: implications for screening and for molecular pathophysiology.

G. Vassart, K. Khoury, J. Dussault, 2002, The Journal of clinical endocrinology and metabolism.

High-dose growth hormone treatment of short children born small for gestational age.

F. de Zegher, L. Breysem, M. Craen, 1996, The Journal of clinical endocrinology and metabolism.

Effects of fasting on the growth plate: systemic and local mechanisms.

J. Baron, J. Yanovski, M. Colli, 1997, Endocrinology.

Phenotypical, biological, and molecular heterogeneity of 5α-reductase deficiency: an extensive international experience of 55 patients.

M. Polak, A. Grüters, Z. Hochberg, 2011, The Journal of clinical endocrinology and metabolism.

Dexamethasone increases growth hormone receptor messenger ribonucleic acid levels in liver and growth plate.

J. Baron, J. Yanovski, C. Heinrichs, 1994, Endocrinology.

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

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

Concerns, Expectations and Perception Regarding Stature, Physical Appearance and Psychosocial Functioning before and during High-Dose Growth Hormone Treatment of Short Pre-pubertal Children Born Small for Gestational Age

C. de Beaufort, Raoul Rooman, M. Craen, 2008, Hormone Research in Paediatrics.

Late or delayed induced or spontaneous puberty in girls with Turner syndrome treated with growth hormone does not affect final height.

M. Craen, C. Heinrichs, G. Massa, 2003, The Journal of clinical endocrinology and metabolism.

Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)

V. Tillmann, P. Chanson, M. Dattani, 2020, Orphanet Journal of Rare Diseases.

Effects of human growth hormone therapy on melanocytic naevi

J. Arrese, J. Bourguignon, C. Heinrichs, 1993, The Lancet.

Consensus Recommendations for the Diagnosis and Management of X-Linked Hypophosphatemia in Belgium

G. Mortier, B. Bravenboer, E. Levtchenko, 2021, Frontiers in 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.

Growth-promoting effect of growth hormone and low dose ethinyl estradiol in girls with Turner's syndrome.

M. Craen, C. Heinrichs, G. Massa, 1990, The Journal of clinical endocrinology and metabolism.

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.

Neurological aspects of hyperinsulinism–hyperammonaemia syndrome

C. Dionisi, F. Escande, E. Roze, 2008, Developmental medicine and child neurology.

Estradiol Levels in Girls with Turner's Syndrome Compared to Normal Prepubertal Girls as Determined by an Ultrasensitive Assay

K. Klein, J. Ross, C. Heinrichs, 2003, Journal of pediatric endocrinology & metabolism : JPEM.

Growth Hormone (GH) Secretion in Patients with Childhood-Onset GH Deficiency: Retesting after One Year of Therapy and at Final Height

M. Craen, C. Heinrichs, G. Massa, 2003, Hormone Research in Paediatrics.

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

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

Congenital central isolated hypothyroidism caused by a homozygous mutation in the TSH-beta subunit gene.

J. Parma, G. Vassart, S. Refetoff, 2000, Thyroid : official journal of the American Thyroid Association.

[Comparison of different MRT techniques in the diagnosis of degenerative cartilage diseases. In vitro study of 50 joint specimens of the knee at T1.5].

M. Rominger, C. Heinrichs, W. Rau, 1997, RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin.

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.

M. Craen, C. Heinrichs, J. Bourguignon, 1998, The Journal of clinical endocrinology and metabolism.

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.

Medullary nephrocalcinosis in nephropathic cystinosis

T. Shawker, W. Gahl, C. Heinrichs, 1995, Pediatric Nephrology.

Thyroid dyshormonogenesis: severe hypothyroidism after normal neonatal thyroid stimulating hormone screening

C. Heinrichs, F. Zegher, G. Vliet, 1992, Acta paediatrica.

A novel approach in the intraoperative management of ovotesticular DSD.

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

NNT mutations: a cause of primary adrenal insufficiency, oxidative stress and extra-adrenal defects.

X. Bertagna, Y. Morel, C. Heinrichs, 2016, European journal of endocrinology.

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.

Congenital Hypothyroidism: A 2020–2021 Consensus Guidelines Update—An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology

D. Luton, M. Polak, H. Krude, 2020, Thyroid : official journal of the American Thyroid Association.

FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly

N. Simonis, G. Mortier, Nelle Lambert, 2013, Journal of Medical Genetics.

Final Height in Children with Idiopathic Growth Hormone Deficiency Treated with Recombinant Human Growth Hormone: The Belgian Experience

Raoul Rooman, F. de Zegher, M. Craen, 2001, Hormone Research in Paediatrics.

Longitudinal study of behavioral and affective patterns in girls with central precocious puberty during long‐acting triptorelin therapy

M. Craen, C. Heinrichs, J. Bourguignon, 1997, Acta paediatrica.

Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci.

C. Gicquel, Y. Le Bouc, S. Cabrol, 2009, Human molecular genetics.

Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences

Y. Le Bouc, S. Chantot-Bastaraud, J. Siffroi, 2017, Journal of Medical Genetics.

Linkage of the gene for the triple A syndrome to chromosome 12q13 near the type II keratin gene cluster.

H J Dean, T. Wienker, D. Easton, 1996, Human molecular genetics.

Fetal hypopituitarism: perinatal endocrine and morphological studies in two cases

C. Christophe, C. Heinrichs, F. Frankenne, 1994, Acta paediatrica.

Sonographic diagnosis of fetal adrenal hyperplasia: utility for prenatal corticotherapy

F. Avni, M. Cassart, C. Donner, 2005, Prenatal diagnosis.

Clinical, hormonal and imaging findings in 27 children with central diabetes insipidus

C. Christophe, C. Heinrichs, G. Massa, 2006, European Journal of Pediatrics.

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

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

Familial adrenocortiocotropin unresponsiveness associated With alacrima and achalasia: Biochemical and molecular studies in two siblings with clincial heterogeneity

G. Chrousos, C. Heinrichs, C. Dugardeyn, 1995, European Journal of Pediatrics.

Gender differences and inflammation: an in vitro model of blood cells stimulation in prepubescent children

N. Lefèvre, J. Désir, C. Heinrichs, 2010, Journal of Inflammation.

DNA methylation profiling and genomic analysis in 20 children with short stature who were born small-for-gestational age.

K. Devriendt, G. Mortier, Raoul Rooman, 2020, The Journal of clinical endocrinology and metabolism.

Six Novel Variants in the MKRN3 Gene Causing Central Precocious Puberty

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

Alu‐element insertion in the homeodomain of HESX1 and aplasia of the anterior pituitary

S. Amselem, I. Netchine, N. Thibaud, 2005, Human mutation.

Sonographic Appearance of Congenital Adrenal Hyperplasia In Utero

F. Avni, C. Heinrichs, Evelyne Diane Chambrier, 2002, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Early, discontinuous, high dose growth hormone treatment to normalize height and weight of short children born small for gestational age: results over 6 years.

F. de Zegher, M. Craen, R. Rosenfeld, 1999, The Journal of clinical endocrinology and metabolism.

Quality of life and retrospective perception of the effect of growth hormone treatment in adult patients with childhood growth hormone deficiency.

F. de Zegher, M. Craen, C. Heinrichs, 2001, Journal of pediatric endocrinology & metabolism : JPEM.

Granulomatous gastritis in Wegener's disease: differentiation from Crohn's disease supported by a positive test for antineutrophil antibodies.

C. Heinrichs, W. Seeger, B. Temmesfeld-Wollbrueck, 1997, Gut.

Variations in pituitary—gonadal suppression during intranasal buserelin and intramuscular depot‐triptorelin therapy for central precocious puberty

M. Craen, C. Heinrichs, J. Bourguignon, 1994, Acta paediatrica.

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

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

Blood spot follicle-stimulating hormone during early postnatal life in normal girls and Turner's syndrome.

J. Bourguignon, C. Heinrichs, P. Bourdoux, 1994, The Journal of clinical endocrinology and metabolism.

Hartsfield holoprosencephaly–ectrodactyly syndrome in five male patients: Further delineation and review

G. Mortier, A. Verloes, C. Baumann, 2009, American journal of medical genetics. Part A.

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.

The role of Doppler evaluation of the uterine artery in girls around puberty

C. Heinrichs, F. Ziereisen, D. Dufour, 2001, Pediatric Radiology.

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.

Familial adrenocorticotropin unresponsiveness associated with alacrima and achalasia: biochemical and molecular studies in two siblings with clinical heterogeneity.

C. Tsigos, G. Chrousos, C. Heinrichs, 1995, European journal of pediatrics.

C. de Beaufort, Raoul Rooman, M. Craen, 2008, Hormone Research in Paediatrics.

Influence of spontaneous or induced puberty on the growth promoting effect of treatment with growth hormone in girls with Turner's syndrome

M. Craen, C. Heinrichs, G. Massa, 1993, Clinical endocrinology.