H. Stöss

发表

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

A. Winterpacht, B. Zabel, A. Superti-Furga, 1996, American journal of medical genetics.

Schimke immuno-osseous dysplasia: a newly recognized multisystem disease.

W. Thoenes, D. Wargowski, G. Hinkel, 1991, The Journal of pediatrics.

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

R. Brenner, P. Müller, U. Vetter, 1993, European Journal of Pediatrics.

Pathomorphological and biochemical alterations in Ehlers-Danlos-syndrome type IV.

A. Nerlich, T. Krieg, H. Lehmann, 1994, Pathology, research and practice.

[Hydrolethalus syndrome].

R. Pfeiffer, K. E. Henkel, H. Stöss, 1993, Der Pathologe.

Cell types infected in human cytomegalovirus placentitis identified by immunohistochemical double staining

T. Löning, B. Plachter, G. Jahn, 2005, Virchows Archiv A.

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

C. Poets, A. Sewell, B. Pontz, 1996, American journal of medical genetics.

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.

A. Winterpacht, B. Zabel, A. Superti-Furga, 1996, Journal of medical genetics.

Progressive pseudorheumatoid arthritis of childhood (PPAC)

C. Bartsocas, J. Spranger, F. Schilling, 1983, European Journal of Pediatrics.

[Genetic-morphologic fatal syndromes. Fetal akinesia sequence (Pena-Shokeir syndrome I)].

R. Pfeiffer, K. E. Henkel, H. Stöss, 1993, Der Pathologe.

Sudden unexpected death in young adults with chronic hydrocephalus

F. Grabellus, W. Paulus, C. Rickert, 2001, International Journal of Legal Medicine.

[Osteoglophonic skeletal dysplasia--a variant of generalized fibrous dysplasia? Case report and review of the literature].

H. Tietze, H. Stöss, E. Sieber, 1991, Der Pathologe.

Preferential cellular and humoral immune reactivities to native and denatured collagen types IX and XI in a patient with fatal relapsing polychondritis.

G. Burmester, H. Burkhardt, J. Kalden, 1993, The Journal of rheumatology.

Are bowing of long tubular bones and preaxial polydactyly signs of the Meckel syndrome?

F. Majewski, T. Goecke, H. Kemperdick, 2004, Human Genetics.

Clinical and ultrastructural findings in three patients with geleophysic dysplasia.

F. Henschke, A. Karbowski, B. Pontz, 1996, American journal of medical genetics.

Intoxication following the inhalation of hydrogen fluoride

A Zober, A. Zober, J Braun, 1984, Archives of Toxicology.

[Dyssegmental dysplasia. Clinical case report and review of literature].

H. Stöss, 1985, Der Pathologe.

A new type of leukoencephalopathy with metaphyseal chondrodysplasia maps to Xq25-q27

U. Stephani, J. Bohl, C. Hübner, 2006, Neurology.

Biochemical, morphological and immunological findings in a patient with a cutis laxa-associated inborn disorder (De Barsy syndrome)

B. Pontz, F. Zepp, H. Stöss, 1986, European Journal of Pediatrics.

Absence of fibula and ulna with oligodactyly, contractures, right-angle bowing of femora, abnormal facial morphology, cleft lip/palate and brain malformation in two sibs: a possibly new lethal syndrome.

G. Wündisch, R. Pfeiffer, H. Stöss, 1988, American journal of medical genetics.

Achondrogenesis Type IA (Houston-Harris): A Still-Unresolved Molecular Phenotype

T. Aigner, T. Rau, C. Thiel, 2007, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.