Hausser I - Search Results

1

Blaschke S, Möller R, Hausser I, Anton-Lamprecht I, Paul E. Blaschke S, et al. Among authors: hausser i. Hautarzt. 1998 Jun;49(6):499-504. doi: 10.1007/s001050050778. Hautarzt. 1998. PMID: 9675580 Review. German.

2

[Hyalinosis cutis et mucosae and Ehlers-Danlos syndrome. A rare combination of syndromes].

König I, Hausser I, Anton-Lamprecht I, Schröter R, Petzoldt D. König I, et al. Among authors: hausser i. Hautarzt. 1994 Feb;45(2):108-12. doi: 10.1007/s001050050049. Hautarzt. 1994. PMID: 7512082 German.

3

[Olmsted syndrome. Successful therapy by treatment with etretinate].

Hausser I, Frantzmann Y, Anton-Lamprecht I, Estes S, Frosch PJ. Hausser I, et al. Hautarzt. 1993 Jun;44(6):394-400. Hautarzt. 1993. PMID: 8335464 German.

4

[Hyalinosis cutis et mucosae (Urbach-Wiethe disease)--ultrastructural and immunological characteristics].

Hausser I, Biltz S, Rauterberg E, Frosch PJ, Anton-Lamprecht I. Hausser I, et al. Hautarzt. 1991 Jan;42(1):28-33. Hautarzt. 1991. PMID: 2010284 German.

5

[Successful retinoid therapy of Netherton syndrome].

Hartschuh W, Hausser I, Petzoldt D. Hartschuh W, et al. Among authors: hausser i. Hautarzt. 1989 Jul;40(7):430-3. Hautarzt. 1989. PMID: 2527214 German.

6

Netherton's syndrome: ultrastructure of the active lesion under retinoid therapy.

Hausser I, Anton-Lamprecht I, Hartschuh W, Petzoldt D. Hausser I, et al. Arch Dermatol Res. 1989;281(3):165-72. doi: 10.1007/BF00456387. Arch Dermatol Res. 1989. PMID: 2528332

7

Severe congenital generalized exfoliative erythroderma in newborns and infants: a possible sign of Netherton syndrome.

Hausser I, Anton-Lamprecht I. Hausser I, et al. Pediatr Dermatol. 1996 May-Jun;13(3):183-99. doi: 10.1111/j.1525-1470.1996.tb01202.x. Pediatr Dermatol. 1996. PMID: 8806118

8

Early preclinical diagnosis of dominant pseudoxanthoma elasticum by specific ultrastructural changes of dermal elastic and collagen tissue in a family at risk.

Hausser I, Anton-Lamprecht I. Hausser I, et al. Hum Genet. 1991 Oct;87(6):693-700. doi: 10.1007/BF00201728. Hum Genet. 1991. PMID: 1937472

9

Differential ultrastructural aberrations of collagen fibrils in Ehlers-Danlos syndrome types I-IV as a means of diagnostics and classification.

Hausser I, Anton-Lamprecht I. Hausser I, et al. Hum Genet. 1994 Apr;93(4):394-407. doi: 10.1007/BF00201664. Hum Genet. 1994. PMID: 8168810

10

Acute bilateral renal vein thrombosis complicating Netherton syndrome.

Pohl M, Zimmerhackl LB, Hausser I, Ludwig H, Hildebrandt F, Gordjani N, Sutor AH, Anton-Lamprecht I, Brandis M. Pohl M, et al. Among authors: hausser i. Eur J Pediatr. 1998 Feb;157(2):157-60. doi: 10.1007/s004310050789. Eur J Pediatr. 1998. PMID: 9504792

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