C. Heinrichs

Details der Publikationsliste

Zeitraum

1993 - 2005

Anzahl

33

Co-Autoren

Trends in age at diagnosis of Turner syndrome (2005)

Verlinde, F, Bourguignon, J P, Craen, M, ...

The age at diagnosis of 242 girls with Turner syndrome (TS) treated in Belgium with growth hormone between 1991 and 2002 was evaluated. The median (range) age at diagnosis was 6.6 (0-18.3) years....

Prevalence and demographic features of childhood growth hormone deficiency in Belgium during the period 1986-2001 (2004)

Massa, G, Craen, M, Bourguignon, J P, Heinrichs, C, ...

OBJECTIVE: Since the availability of recombinant human growth hormone (rhGH) all children with growth hormone deficiency (GHD) living in Belgium are offered rhGH treatment after approval by a...

Late or delayed induced or spontaneous puberty in girls with Turner syndrome treated with growth hormone does not affect final height (2003)

Heinrichs, C, Verlinde, Siska, Thomas, Muriel, Bourguignon, JP, Craen, M, ...

Although it has been well established that GH treatment increases final height (FH) in girls with Turner syndrome (TS), the optimal ages to start GH therapy and introduce estrogens for pubertal...

Growth hormone (GH) secretion in patients with childhood-onset GH deficiency: Retesting after one year of therapy and at final height (2003)

Massa, G, Maes, M, Beckers, D, Craen, M, Francois, I, ...

Background. Recent studies have shown that many patients treated with growth hormone (GH) during childhood because of idiopathic GH deficiency (GHD) are no longer GH deficient when retested after...

Sexual Precocity after Immigration from Developing Countries to Belgium: Evidence of Previous Exposure to Organochlorine Pesticides (2001)

Krstevska-Konstantinova, M, Charlier, Corinne, Craen, M, Du Caju, M, Heinrichs, C, De Beaufort, C, ...

In a retrospective auxological study of 145 patients seen in Belgium during a 9-year period for treatment of precocious puberty, 28% appeared to be foreign children (39 girls, one boy) who immigrated...

Final height in children with idiopathic growth hormone deficiency treated with recombinant human growth hormone: The Belgian experience (2001)

Massa, G, Bourguignon, JP, Craen, M, De Schepper, J, ...

Background: The growth response to recombinant hGH (rhGH) treatment and final height of 61 Belgian children (32 boys) with idiopathic growth hormone deficiency (GHD) were studied. Patients/Methods:...

Sexual precocity after immigration from developing countries to Belgium: evidence of previous exposure to organochlorine pesticides (2001)

Krstevska-Konstantinova, M., Charlier, C., Craen, M., Du Caju, M., Heinrichs, C., De Beaufort, C., ...

In a retrospective auxological study of 145 patients seen in Belgium during a 9-year period for treatment of precocious puberty, 28% appeared to be foreign children (39 girls, one boy) who immigrated...

Early, discontinuous, high dose growth hormone treatment to normalize height and weight of short children born small for gestational age: Results over 6 years (1999)

Du Caju, MVL, Heinrichs, C, De Schepper, J, Craen, M, ...

Most children born small for gestational age (SGA) normalize their size through spontaneous catch-up growth within the first 2 yr after birth. Some SGA children fail to do so and maintain an...

High-dose growth hormone treatment of short children born small for gestational age (1996)

Gargosky, SE, Heinrichs, C, DuCaju, MVL, Thiry, G, ...

The effect of GH administration was evaluated over 2 yr in 50 short, prepubertal, non-GH deficient children born small for gestational age, who had been randomly allocated to a group receiving no...

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

Abramowicz, M J, Duprez, L, Parma, J, Vassart, G, Heinrichs, C

Thyroid gland agenesis is the most common cause of congenital hypothyroidism and is usually sporadic. We investigated a brother and sister from consanguineous parents, ascertained through systematic...

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

Abramowicz, M J, Duprez, L, Parma, J, Vassart, G, Heinrichs, C

Thyroid gland agenesis is the most common cause of congenital hypothyroidism and is usually sporadic. We investigated a brother and sister from consanguineous parents, ascertained through systematic...

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

Temmesfeld-Wollbrueck, B, Heinrichs, C, Szalay, A, Seeger, W

BACKGROUND: This report concerns the gastric manifestation of Wegener's granulomatosis in a 44 year old white female patient who initially presented with abdominal pain, vomiting, and iridocyclitis....