Craen M - Search Results

1

Acute suppurative thyroiditis complicating second allogeneic transplant for juvenile CMML.

Poelman M, Benoit Y, Laureys G, Craen M, Leroy J. Poelman M, et al. Among authors: craen m. Bone Marrow Transplant. 1992 Dec;10(6):547-8. Bone Marrow Transplant. 1992. PMID: 1490204

2

Factors contributing to the impairment of growth in children with acute lymphoblastic leukemia.

Logghe KA, Bourguignon JP, Craen M, Benoit Y. Logghe KA, et al. Among authors: craen m. Horm Res. 1988;30(2-3):62-7. doi: 10.1159/000181030. Horm Res. 1988. PMID: 3248778 Free article.

3

De novo terminal deletion 7p22.1--pter in a child without craniosynostosis.

Speleman F, Craen M, Leroy J. Speleman F, et al. Among authors: craen m. J Med Genet. 1989 Aug;26(8):528-32. doi: 10.1136/jmg.26.8.528. J Med Genet. 1989. PMID: 2671374 Free PMC article. Review.

4

Gender difference in aerobic capacity in adolescents after cure from malignant disease in childhood.

Matthys D, Verhaaren H, Benoit Y, Laureys G, De Naeyer A, Craen M. Matthys D, et al. Among authors: craen m. Acta Paediatr. 1993 May;82(5):459-62. doi: 10.1111/j.1651-2227.1993.tb12722.x. Acta Paediatr. 1993. PMID: 8518522

5

On the variability of the Brachmann-de Lange syndrome in seven patients.

Leroy JG, Persijn J, Van de Weghe V, Van Hecke R, Oostra A, De Bie S, Craen M. Leroy JG, et al. Among authors: craen m. Am J Med Genet. 1993 Nov 15;47(7):983-91. doi: 10.1002/ajmg.1320470709. Am J Med Genet. 1993. PMID: 8291541

6

Identification and characterization of normal length nonfluorescent Y chromosomes: cytogenetic analysis, southern hybridization and non-isotopic in situ hybridization.

Speleman F, Van der Auwera B, Mangelschots K, Vercruyssen M, Raap T, Wiegant J, Craen M, Leroy J. Speleman F, et al. Among authors: craen m. Hum Genet. 1990 Oct;85(6):569-75. doi: 10.1007/BF00193576. Hum Genet. 1990. PMID: 2227946

7

Familial deficiency of growth hormone and spinal muscular atrophy.

Leroy JG, Craen MM. Leroy JG, et al. Among authors: craen mm. Prog Clin Biol Res. 1985;200:113-21. Prog Clin Biol Res. 1985. PMID: 2867557 No abstract available.

8

Extra Yq and partial monosomy 12p due to a Y;12 translocation in a boy with features of the 12p deletion syndrome.

Orye E, Craen M, Laureys G, van Coster R, van Mele B. Orye E, et al. Among authors: craen m. J Med Genet. 1985 Jun;22(3):222-4. doi: 10.1136/jmg.22.3.222. J Med Genet. 1985. PMID: 4009644 Free PMC article.

9

Clinical and radiographic features of a family with hypochondroplasia owing to a novel Asn540Ser mutation in the fibroblast growth factor receptor 3 gene.

Mortier G, Nuytinck L, Craen M, Renard JP, Leroy JG, de Paepe A. Mortier G, et al. Among authors: craen m. J Med Genet. 2000 Mar;37(3):220-4. doi: 10.1136/jmg.37.3.220. J Med Genet. 2000. PMID: 10777366 Free PMC article. No abstract available.

10

Growth hormone therapy in pre-pubertal children with Noonan syndrome: first year growth response and comparison with Turner syndrome.

De Schepper J, Otten BJ, François I, Bourguignon JP, Craen M, Van der Burgt I, Massa GG. De Schepper J, et al. Among authors: craen m. Acta Paediatr. 1997 Sep;86(9):943-6. doi: 10.1111/j.1651-2227.1997.tb15175.x. Acta Paediatr. 1997. PMID: 9343272 Free article.

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