Spranger J - Search Results

1

Osteogenesis imperfecta and hyperplastic callus formation: light- and electron-microscopic findings.

Stöss H, Pontz B, Vetter U, Karbowski A, Brenner R, Spranger J. Stöss H, et al. Among authors: spranger j. Am J Med Genet. 1993 Jan 15;45(2):260. doi: 10.1002/ajmg.1320450222. Am J Med Genet. 1993. PMID: 8456814

2

Clinical and ultrastructural findings in three patients with geleophysic dysplasia.

Pontz BF, Stöss H, Henschke F, Freisinger P, Karbowski A, Spranger J. Pontz BF, et al. Among authors: spranger j. Am J Med Genet. 1996 May 3;63(1):50-4. doi: 10.1002/(SICI)1096-8628(19960503)63:1<50::AID-AJMG11>3.0.CO;2-T. Am J Med Genet. 1996. PMID: 8723086

3

Heterogeneity in osteogenesis imperfecta: clinical and morphological findings.

Pontz BF, Stöss H, Spranger J. Pontz BF, et al. Among authors: spranger j. Ann N Y Acad Sci. 1988;543:30-9. doi: 10.1111/j.1749-6632.1988.tb55313.x. Ann N Y Acad Sci. 1988. PMID: 3214051 No abstract available.

4

A specific collagen type II gene (COL2A1) mutation presenting as spondyloperipheral dysplasia.

Zabel B, Hilbert K, Stöss H, Superti-Furga A, Spranger J, Winterpacht A. Zabel B, et al. Among authors: spranger j. Am J Med Genet. 1996 May 3;63(1):123-8. doi: 10.1002/(SICI)1096-8628(19960503)63:1<123::AID-AJMG22>3.0.CO;2-P. Am J Med Genet. 1996. PMID: 8723097

5

[Treatment of osteogenesis imperfecta with (+)-catechin (author's transl)].

Stöss H, Pesch HJ, Spranger J. Stöss H, et al. Among authors: spranger j. Dtsch Med Wochenschr. 1979 Dec 14;104(50):1774, 1777-8. doi: 10.1055/s-0028-1129189. Dtsch Med Wochenschr. 1979. PMID: 510214 German.

6

[Osteogenesis imperfecta in childhood and adolescence].

Brenner RE, Schiller B, Pontz BF, Lehmann H, Teller WM, Spranger J, Vetter U. Brenner RE, et al. Among authors: spranger j. Monatsschr Kinderheilkd. 1993 Dec;141(12):940-5. Monatsschr Kinderheilkd. 1993. PMID: 8114777 German.

7

Osteogenesis imperfecta: a clinical study of the first ten years of life.

Vetter U, Pontz B, Zauner E, Brenner RE, Spranger J. Vetter U, et al. Among authors: spranger j. Calcif Tissue Int. 1992 Jan;50(1):36-41. doi: 10.1007/BF00297295. Calcif Tissue Int. 1992. PMID: 1739868

8

The deletion of six amino acids at the C-terminus of the alpha 1 (II) chain causes overmodification of type II and type XI collagen: further evidence for the association between small deletions in COL2A1 and Kniest dysplasia.

Winterpacht A, Superti-Furga A, Schwarze U, Stöss H, Steinmann B, Spranger J, Zabel B. Winterpacht A, et al. Among authors: spranger j. J Med Genet. 1996 Aug;33(8):649-54. doi: 10.1136/jmg.33.8.649. J Med Genet. 1996. PMID: 8863156 Free PMC article.

9

[Differential diagnosis of primary constitutional osteopenias. Light and electron microscopy findings].

Stöss H, Spranger J. Stöss H, et al. Among authors: spranger j. Internist (Berl). 1985 Aug;26(8):491-501. Internist (Berl). 1985. PMID: 3902706 German. No abstract available.

10

Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studies.

Opitz JM, Spranger JW, Stöss HR, Pesch HJ, Azadeh B. Opitz JM, et al. Among authors: spranger jw. Am J Med Genet. 1987 Mar;26(3):583-90. doi: 10.1002/ajmg.1320260312. Am J Med Genet. 1987. PMID: 3565474

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