Stöss H - 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. Am J Med Genet. 1993 Jan 15;45(2):260. doi: 10.1002/ajmg.1320450222. Am J Med Genet. 1993. PMID: 8456814

2

Heterogeneity in osteogenesis imperfecta: clinical and morphological findings.

Pontz BF, Stöss H, Spranger J. Pontz BF, et al. Among authors: stoss h. 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.

3

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: stoss h. 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

4

Defective collagen fibril formation and mineralization in osteogenesis imperfecta with congenital joint contractures (Bruck syndrome).

Brenner RE, Vetter U, Stöss H, Müller PK, Teller WM. Brenner RE, et al. Among authors: stoss h. Eur J Pediatr. 1993 Jun;152(6):505-8. doi: 10.1007/BF01955060. Eur J Pediatr. 1993. PMID: 8335019

5

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

Stöss H, Pesch HJ, Spranger J. Stöss H, et al. 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

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: stoss h. 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

7

The spectrum of free neuraminic acid storage disease in childhood: clinical, morphological and biochemical observations in three non-Finnish patients.

Sewell AC, Poets CF, Degen I, Stöss H, Pontz BF. Sewell AC, et al. Among authors: stoss h. Am J Med Genet. 1996 May 3;63(1):203-8. doi: 10.1002/(SICI)1096-8628(19960503)63:1<203::AID-AJMG36>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8723111

8

Collagen fibrils of osteoid in osteogenesis imperfecta: morphometrical analysis of the fibril diameter.

Stöss H, Freisinger P. Stöss H, et al. Am J Med Genet. 1993 Jan 15;45(2):257. doi: 10.1002/ajmg.1320450220. Am J Med Genet. 1993. PMID: 8456812

9

Heterogeneity of osteogenesis imperfecta. Biochemical and morphological findings in a case of type III according to Sillence.

Stöss H, Pontz BF, Pesch HJ, Ott R. Stöss H, et al. Eur J Pediatr. 1986 Apr;145(1-2):34-9. doi: 10.1007/BF00441849. Eur J Pediatr. 1986. PMID: 3732329

10

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

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

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