Goossens M - Search Results

1

Very late immune response to growth hormone (GH) therapy in an infant with GH-N gene deletion.

De Luca F, Duquesnoy P, Arrigo T, Lombardo F, Goossens M. De Luca F, et al. Among authors: goossens m. Acta Paediatr. 1992 Sep;81(9):730. doi: 10.1111/j.1651-2227.1992.tb12350.x. Acta Paediatr. 1992. PMID: 1294098 No abstract available.

2

Point mutations in the growth hormone receptor gene of patients with Laron syndrome.

Amselem S, Duriez B, Sobrier ML, Duquesnoy P, Goossens M. Amselem S, et al. Among authors: goossens m. Acta Paediatr Suppl. 1992 Sep;383:132-3. Acta Paediatr Suppl. 1992. PMID: 1458008 Review. No abstract available.

3

Long-lasting catch-up growth under bio-methionyl growth hormone treatment in an infant with isolated growth hormone deficiency type 1A.

De Luca F, Duquesnoy P, Arrigo T, Lombardo F, Goossens M. De Luca F, et al. Among authors: goossens m. Acta Paediatr Scand. 1991 Dec;80(12):1235-40. doi: 10.1111/j.1651-2227.1991.tb11816.x. Acta Paediatr Scand. 1991. PMID: 1686134

4

Molecular defects in the growth hormone receptor.

Amselem S, Duquesnoy P, Sobrier ML, Goossens M. Amselem S, et al. Among authors: goossens m. Acta Paediatr Scand Suppl. 1991;377:81-6. doi: 10.1111/apa.1991.80.s377.81. Acta Paediatr Scand Suppl. 1991. PMID: 1785318 Review. No abstract available.

5

Isolated growth hormone (GH) deficiency type 1A associated with a double deletion in the human GH gene cluster.

Goossens M, Brauner R, Czernichow P, Duquesnoy P, Rappaport R. Goossens M, et al. J Clin Endocrinol Metab. 1986 Apr;62(4):712-6. doi: 10.1210/jcem-62-4-712. J Clin Endocrinol Metab. 1986. PMID: 3005356

6

Isolated growth hormone deficiency type IA associated with a 45-kilobase gene deletion within the human growth hormone gene cluster in an Italian family.

Ghizzoni L, Duquesnoy P, Torresani T, Vottero A, Goossens M, Bernasconi S. Ghizzoni L, et al. Among authors: goossens m. Pediatr Res. 1994 Nov;36(5):654-9. doi: 10.1203/00006450-199411000-00021. Pediatr Res. 1994. PMID: 7877887

7

Molecular genetics of Laron-type GH insensitivity syndrome.

Goossens M, Amselem S, Duquesnoy P, Sobrier ML. Goossens M, et al. Recent Prog Horm Res. 1993;48:165-78. doi: 10.1016/b978-0-12-571148-7.50010-5. Recent Prog Horm Res. 1993. PMID: 8441847 Review. No abstract available.

8

Molecular basis of inherited growth hormone resistance in childhood.

Amselem S, Sobrier ML, Dastot F, Duquesnoy P, Duriez B, Goossens M. Amselem S, et al. Among authors: goossens m. Baillieres Clin Endocrinol Metab. 1996 Jul;10(3):353-69. doi: 10.1016/s0950-351x(96)80485-x. Baillieres Clin Endocrinol Metab. 1996. PMID: 8853444 Review.

9

Nine novel growth hormone receptor gene mutations in patients with Laron syndrome.

Sobrier ML, Dastot F, Duquesnoy P, Kandemir N, Yordam N, Goossens M, Amselem S. Sobrier ML, et al. Among authors: goossens m. J Clin Endocrinol Metab. 1997 Feb;82(2):435-7. doi: 10.1210/jcem.82.2.3725. J Clin Endocrinol Metab. 1997. PMID: 9024232

10

[Molecular genetics of growth hormone resistance syndrome].

Amselem S, Duriez B, Duquesnoy P, Sobrier ML, Goossens M. Amselem S, et al. Among authors: goossens m. C R Seances Soc Biol Fil. 1992;186(4):354-62. C R Seances Soc Biol Fil. 1992. PMID: 1301223 Review. French.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

557 results

Search Page

Filters