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Ingrun Anton-Lamprecht

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J Dahlqvist; Joakim Klar; Ingrid Hausser; Ingrun Anton-Lamprecht; Maritta Pigg; Tobias Gedde-Dahl; Agneta Gånemo; Anders Vahlquist; Niklas Dahl
Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis.
Janbernd Kirschner; Ingrid Hausser; Yaqun Zou; Gudrun Schreiber; Hans-Jürgen Christen; Susan C Brown; Ingrun Anton-Lamprecht; Francesco Muntoni; Folker Hanefeld; Carsten G Bönnemann
Ullrich congenital muscular dystrophy: connective tissue abnormalities in the skin support overlap with Ehlers-Danlos syndromes.
Birgit Buchroithner; Alfred Klausegger; Ulrike Ebschner; Ingrun Anton-Lamprecht; Gabriele Pohla-Gubo; Christoph M Lanschuetzer; Markus Laimer; Helmut Hintner; Johann W Bauer
Analysis of the LAMB3 gene in a junctional epidermolysis bullosa patient reveals exonic splicing and allele-specific nonsense-mediated mRNA decay.

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2007: J Dahlqvist; Joakim Klar; Ingrid Hausser; Ingrun Anton-Lamprecht; Maritta Pigg; Tobias Gedde-Dahl; Agneta Gånemo; Anders Vahlquist; Niklas Dahl
Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis.
Journal of medical genetics 2007;44(10):615-20.
2005: Janbernd Kirschner; Ingrid Hausser; Yaqun Zou; Gudrun Schreiber; Hans-Jürgen Christen; Susan C Brown; Ingrun Anton-Lamprecht; Francesco Muntoni; Folker Hanefeld; Carsten G Bönnemann
Ullrich congenital muscular dystrophy: connective tissue abnormalities in the skin support overlap with Ehlers-Danlos syndromes.
American journal of medical genetics. Part A 2005;132A(3):296-301.
2004: Birgit Buchroithner; Alfred Klausegger; Ulrike Ebschner; Ingrun Anton-Lamprecht; Gabriele Pohla-Gubo; Christoph M Lanschuetzer; Markus Laimer; Helmut Hintner; Johann W Bauer
Analysis of the LAMB3 gene in a junctional epidermolysis bullosa patient reveals exonic splicing and allele-specific nonsense-mediated mRNA decay.
Laboratory investigation; a journal of technical methods and pathology 2004;84(10):1279-88.
2002: Dörte Koss-Harnes; Bjørn Høyheim; Ingrun Anton-Lamprecht; Aud Gjesti; Randi S Jørgensen; Frode L Jahnsen; Bjørnar Olaisen; Gerhard Wiche; Tobias Gedde-Dahl
A site-specific plectin mutation causes dominant epidermolysis bullosa simplex Ogna: two identical de novo mutations.
The Journal of investigative dermatology 2002;118(1):87-93.
1998: Maritta Pigg; Tobias Gedde-Dahl; D Cox; Ingrid Hausser; Ingrun Anton-Lamprecht; Niklas Dahl
Strong founder effect for a transglutaminase 1 gene mutation in lamellar ichthyosis and congenital ichthyosiform erythroderma from Norway.
European journal of human genetics : EJHG 1998;6(6):589-96.
1998: Tobias Brandt; Ingrid Hausser; E Orberk; Armin Grau; W Hartschuh; Ingrun Anton-Lamprecht; Werner Hacke
Ultrastructural connective tissue abnormalities in patients with spontaneous cervicocerebral artery dissections.
Annals of neurology 1998;44(2):281-5.
1998: S Blaschke; R Möller; Ingrid Hausser; Ingrun Anton-Lamprecht; E Paul
[Comèl-Netherton syndrome].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 1998;49(6):499-504.
1998: M Pohl; Lothar B Zimmerhackl; Ingrid Hausser; H Ludwig; Friedhelm Hildebrandt; Nader Gordjani; Anton Heinz Sutor; Ingrun Anton-Lamprecht; Matthias Brandis
Acute bilateral renal vein thrombosis complicating Netherton syndrome.
European journal of pediatrics 1998;157(2):157-60.
1997: N Hammami-Hauasli; D U Kalinke; Hauke Schumann; U Kalinke; B F Pontz; Ingrun Anton-Lamprecht; L Pulkkinen; M Zimmermann; J Uitto; Leena Bruckner-Tuderman
A combination of a common splice site mutation and a frameshift mutation in the COL7A1 gene: absence of functional collagen VII in keratinocytes and skin.
The Journal of investigative dermatology 1997;109(3):384-9.
1997: Jan-Olof Winberg; N Hammami-Hauasli; Oivind Nilssen; Ingrun Anton-Lamprecht; Susan Naylor; K Kerbacher; M Zimmermann; P Krajci; Tobias Gedde-Dahl; Leena Bruckner-Tuderman
Modulation of disease severity of dystrophic epidermolysis bullosa by a splice site mutation in combination with a missense mutation in the COL7A1 gene.
Human molecular genetics 1997;6(7):1125-35.
1997: Anne De Paepe; Lieve Nuytinck; Ingrid Hausser; Ingrun Anton-Lamprecht; J M Naeyaert
Mutations in the COL5A1 gene are causal in the Ehlers-Danlos syndromes I and II.
American journal of human genetics 1997;60(3):547-54.
1996: Sigrid Tinschert; Ingrun Anton-Lamprecht; H Albrecht-Nebe; Heike Audring
Zunich neuroectodermal syndrome: migratory ichthyosiform dermatosis, colobomas, and other abnormalities.
Pediatric dermatology 1996;13(5):363-71.
1996: Ingrid Hausser; Ingrun Anton-Lamprecht
Severe congenital generalized exfoliative erythroderma in newborns and infants: a possible sign of Netherton syndrome.
Pediatric dermatology 1996;13(3):183-99.
1994: D Krahl; A Sigwart; Wolfgang Hartschuh; Ingrun Anton-Lamprecht; Detlef Petzoldt
[Erythrokeratolysis hiemalis. Erythematosquamous genetic dermatosis with seasonal manifestation].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 1994;45(11):776-9.
1994: Ingrun Anton-Lamprecht
Ultrastructural identification of basic abnormalities as clues to genetic disorders of the epidermis.
The Journal of investigative dermatology 1994;103(5 Suppl):6S-12S.
1994: Ingrun Anton-Lamprecht; R Rauskolb
[Prenatal diagnosis of genetic dermatoses].
Der Gynäkologe 1994;27(5):296-308.
1994: T Gedde-Dahl; B M Dupuy; R Jonassen; Jan-Olof Winberg; Ingrun Anton-Lamprecht; Bjørnar Olaisen
Junctional epidermolysis bullosa inversa (locus EBR2A) assigned to 1q31 by linkage and association to LAMC1.
Human molecular genetics 1994;3(8):1387-91.
1994: Ingrid Hausser; Ingrun Anton-Lamprecht
Differential ultrastructural aberrations of collagen fibrils in Ehlers-Danlos syndrome types I-IV as a means of diagnostics and classification.
Human genetics 1994;93(4):394-407.
1994: I König; Ingrid Hausser; Ingrun Anton-Lamprecht; R Schröter; Detlef Petzoldt
[Hyalinosis cutis et mucosae and Ehlers-Danlos syndrome. A rare combination of syndromes].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 1994;45(2):108-12.
1993: M L Arnold; Ingrun Anton-Lamprecht
Multiple eruptive cephalic histiocytomas in a case of T-cell lymphoma. A xanthomatous stage of benign cephalic histiocytosis in an adult patient?
The American Journal of dermatopathology 1993;15(6):581-6.
1993: Ingrid Hausser; Y Frantzmann; Ingrun Anton-Lamprecht; S Estes; Peter J Frosch
[Olmsted syndrome. Successful therapy by treatment with etretinate].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 1993;44(6):394-400.
1993: B Weidenthaler; Ingrid Hausser; Ingrun Anton-Lamprecht
Is filaggrin really a filament-aggregating protein in vivo?
Archives of dermatological research 1993;285(3):111-20.
1992: Leena Bruckner-Tuderman; Jan-Olof Winberg; Ingrun Anton-Lamprecht; U W Schnyder; T Gedde-Dahl
Anchoring fibrils, collagen VII, and neutral metalloproteases in recessive dystrophic epidermolysis bullosa inversa.
The Journal of investigative dermatology 1992;99(5):550-8.
1992: M L Arnold; Ingrun Anton-Lamprecht; H Albrecht-Nebe
Congenital ichthyosis with hypogonadism and growth retardation--a new syndrome with peculiar ultrastructural features.
Archives of dermatological research 1992;284(4):198-208.
1991: Ingrid Hausser; Ingrun Anton-Lamprecht
Early preclinical diagnosis of dominant pseudoxanthoma elasticum by specific ultrastructural changes of dermal elastic and collagen tissue in a family at risk.
Human genetics 1991;87(6):693-700.
1991: Ingrid Hausser; S Biltz; E Rauterberg; Peter J Frosch; Ingrun Anton-Lamprecht
[Hyalinosis cutis et mucosae (Urbach-Wiethe disease)--ultrastructural and immunological characteristics].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 1991;42(1):28-33.
1991: S Günzel; B Weidenthaler; Ingrid Hausser; Ingrun Anton-Lamprecht
Keratohyalin granules are heterogeneous in ridged and non-ridged human skin: evidence from anti-filaggrin immunogold labelling of normal skin and skin of autosomal dominant ichthyosis vulgaris patients.
Archives of dermatological research 1991;283(7):421-32.
1990: Ingrid Hausser; Ingrun Anton-Lamprecht
Prenatal diagnosis of genodermatoses by ultrastructural diagnostic markers in extra-embryonic tissues: defective hemidesmosomes in amnion epithelium of fetuses affected with epidermolysis bullosa Herlitz type (an alternative prenatal diagnosis in certain cases).
Human genetics 1990;85(3):367-75.
1990: I Kastl; Ingrun Anton-Lamprecht; P Gamborg Nielsen
Hereditary palmoplantar keratosis of the Gamborg Nielsen type. Clinical and ultrastructural characteristics of a new type of autosomal recessive palmoplantar keratosis.
Archives of dermatological research 1990;282(6):363-70.
1990: K Schärer; Ingrid Hausser; Ingrun Anton-Lamprecht; W Tilgen
Clinical quiz. Pseudoxanthoma elasticum (PXE).
Pediatric nephrology (Berlin, Germany) 1990;4(1):97-9.
1990: I Kastl; Ingrun Anton-Lamprecht
Bicomponent keratohyalin in normal human ridged skin.
Archives of dermatological research 1990;282(2):71-5.
1989: Ingrid Hausser; Ingrun Anton-Lamprecht; B Gustavii
Prenatal diagnosis of junctional epidermolysis bullosa Herlitz type.
Lancet 1989;2(8670):1035-6.
1989: Ingrid Hausser; Ingrun Anton-Lamprecht; Wolfgang Hartschuh; Detlef Petzoldt
Netherton's syndrome: ultrastructure of the active lesion under retinoid therapy.
Archives of dermatological research 1989;281(3):165-72.
1988: Ingrid Hausser; Ingrun Anton-Lamprecht
Ultrastructure of first trimester chorionic villi with regard to the prenatal diagnosis of genodermatoses.
Prenatal diagnosis 1988;8(7):511-24.
1988: Manige Fartasch; Ingrun Anton-Lamprecht; Peter J Frosch; Detlef Petzoldt
[Polyvinylpyrrolidone dermatoses. Clinical aspects and ultrastructural morphology].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 1988;39(9):569-75.
1988: J F Mann; Martin Zeier; Eugen Zilow; K Schärer; Ingrun Anton-Lamprecht; R Waldherr; Konrad Andrassy; Eberhard Ritz
The spectrum of renal involvement in epidermolysis bullosa dystrophica hereditaria: report of two cases.
American journal of kidney diseases : the official journal of the National Kidney Foundation 1988;11(5):437-41.
1988: K P Steuhl; Ingrun Anton-Lamprecht; M L Arnold; HJ Thiel
[Recurrent corneal erosion in epidermolysis bullosa simplex Köbner and X-chromosomal ichthyosis].
Fortschritte der Ophthalmologie : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft 1988;85(6):669-71.
1988: Ingrun Anton-Lamprecht; E Schleiermacher; M Wolf
Autosomal recessive anhidrotic ectodermal dysplasia: report of a case and discrimination of diagnostic features.
Birth defects original article series 1988;24(2):183-95.
1988: M L Arnold; Ingrun Anton-Lamprecht; B Melz-Rothfuss; Wolfgang Hartschuh
Ichthyosis congenita type III. Clinical and ultrastructural characteristics and distinction within the heterogeneous ichthyosis congenita group.
Archives of dermatological research 1988;280(5):268-78.
1988: K P Steuhl; Ingrun Anton-Lamprecht; M L Arnold; HJ Thiel
Recurrent bilateral corneal erosions due to an association of epidermolysis bullosa simplex Köbner and X-linked ichthyosis with steroid sulfatase deficiency.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 1988;226(3):216-23.
1987: W Bernart; Thomas Rabe; E Schleiermacher; Ingrun Anton-Lamprecht; Benno Runnebaum
Freezing-thawing behaviour and cell membrane ultrastructure of mouse embryos pre-cultured in B2-Menezo medium before cryopreservation.
Human reproduction (Oxford, England) 1987;2(8):679-87.
1987: Ingrid Hausser; Ingrun Anton-Lamprecht
Electron microscopy as a means for carrier detection and genetic counselling in families at risk of tuberous sclerosis.
Human genetics 1987;76(1):73-80.
1987: Ingrun Anton-Lamprecht; M L Arnold
Prenatal diagnosis of inherited epidermolyses.
Current problems in dermatology 1987;16():146-57.
1987: M L Arnold; Ingrun Anton-Lamprecht
Prenatal diagnosis of epidermal disorders.
Current problems in dermatology 1987;16():120-8.
1987: Ingrid Hausser; Manige Fartasch; E Schleiermacher; Ingrun Anton-Lamprecht
Disseminated cicatricial pemphigoid in a child and in an adult. Ultrastructural diagnostic criteria and differential diagnosis with special reference to acquired epidermolysis bullosa.
Archives of dermatological research 1987;279(6):357-65.
1985: M L Arnold; Ingrun Anton-Lamprecht
Problems in prenatal diagnosis of the ichthyosis congenita group.
Human genetics 1985;71(4):301-11.
1984: M L Arnold; R Rauskolb; Ingrun Anton-Lamprecht; A Schinzel; W Schmid
Prenatal diagnosis of anhidrotic ectodermal dysplasia.
Prenatal diagnosis 1984;4(2):85-98.
1982: M L Arnold; H Wirth; Ingrun Anton-Lamprecht; D Petzoldt
[Generalized eruptive histiocytoma].
Der Hautarzt; Zeitschrift für Dermatologie, Venerologie, und verwandte Gebiete 1982;33(8):428-37.
1982: Ingrun Anton-Lamprecht; M L Arnold; R Rauskolb; A Schinzel; W Schmid; U W Schnyder
Prenatal diagnosis of anhydrotic ectodermal dysplasia.
Human genetics 1982;62(2):180.
1981: Ingrun Anton-Lamprecht; R Rauskolb; V Jovanovic; B Kern; M L Arnold; W Schenck
Prenatal diagnosis of epidermolysis bullosa dystrophica Hallopeau-Siemens with electron microscopy of fetal skin.
Lancet 1981;2(8255):1077-9.