Ingrid Hausser

Ingrid Hausser

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Ingrid Hausser

Ingrid Hausser

Publications by authors named "Ingrid Hausser"

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TGFBR2‑dependent alterations of microRNA profiles in extracellular vesicles and parental colorectal cancer cells.

Int J Oncol 2019 Oct 19;55(4):925-937. Epub 2019 Aug 19.

Department of Applied Tumor Biology, Institute of Pathology, Heidelberg University Hospital, D‑69120 Heidelberg, Germany.

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http://dx.doi.org/10.3892/ijo.2019.4859DOI Listing
October 2019

SILAC-Based Quantification of TGFBR2-Regulated Protein Expression in Extracellular Vesicles of Microsatellite Unstable Colorectal Cancers.

Int J Mol Sci 2019 Aug 26;20(17). Epub 2019 Aug 26.

Department Applied Tumor Biology, Institute of Pathology, Heidelberg University Hospital, Im Neuenheimer Feld 224, 69120 Heidelberg, Germany.

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http://dx.doi.org/10.3390/ijms20174162DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6747473PMC
August 2019

SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy.

J Hum Genet 2019 Jul 24;64(7):609-616. Epub 2019 Apr 24.

Institut für Medizinische Genetik und Humangenetik, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.

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http://www.nature.com/articles/s10038-019-0602-8
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http://dx.doi.org/10.1038/s10038-019-0602-8DOI Listing
July 2019

Transcriptome Profiling of Primary Skin Fibroblasts Reveal Distinct Molecular Features Between - and -Kyphoscoliotic Ehlers-Danlos Syndrome.

Genes (Basel) 2019 07 8;10(7). Epub 2019 Jul 8.

Connective Tissue Unit, Division of Metabolism and Children's Research Centre, University Children's Hospital, 8032 Zürich, Switzerland.

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http://dx.doi.org/10.3390/genes10070517DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678841PMC
July 2019

ECM1 Prevents Activation of Transforming Growth Factor β, Hepatic Stellate Cells, and Fibrogenesis in Mice.

Gastroenterology 2019 Jul 27. Epub 2019 Jul 27.

State Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences University of Chinese Academy of Sciences, Shanghai, China; School of Life Science and Technology, Shanghai Tech University, Shanghai, China. Electronic address:

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http://dx.doi.org/10.1053/j.gastro.2019.07.036DOI Listing
July 2019

Clinically Relevant Correction of Recessive Dystrophic Epidermolysis Bullosa by Dual sgRNA CRISPR/Cas9-Mediated Gene Editing.

Mol Ther 2019 May 15;27(5):986-998. Epub 2019 Mar 15.

Department of Biomedical Engineering, Carlos III University (UC3M), Madrid, Spain; Centro de Investigación Biomédica en Red en Enfermedades Raras (CIBERER) U714, Madrid, Spain; Fundación Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz, Madrid, Spain; Epithelial Biomedicine Division, Centro de Investigaciones Energéticas Medioambientales y Tecnológicas (CIEMAT), Madrid, Spain. Electronic address:

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http://dx.doi.org/10.1016/j.ymthe.2019.03.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520462PMC
May 2019

Neue Therapieansätze für entzündliche und bullöse Formen kongenitaler Ichthyosen: erste klinische Erfahrungen.

J Dtsch Dermatol Ges 2019 May;17 Suppl 2:12-15

Klinik für Hautkrankheiten, Universitätsklinikum Münster, Deutschland.

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http://dx.doi.org/10.1111/ddg.13782DOI Listing
May 2019

Constitutional absence of epithelial integrin α3 impacts the composition of the cellular microenvironment of ILNEB keratinocytes.

Matrix Biol 2018 12 3;74:62-76. Epub 2018 Jul 3.

Department of Dermatology, Medical Center - University of Freiburg, Faculty of Medicine, Freiburg, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.matbio.2018.07.001DOI Listing
December 2018

Mutation update for CYP4F22 variants associated with autosomal recessive congenital ichthyosis.

Hum Mutat 2018 10 7;39(10):1305-1313. Epub 2018 Aug 7.

Faculty of Medicine, Institute of Human Genetics, University Medical Center Freiburg, University of Freiburg, Freiburg, Germany.

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http://dx.doi.org/10.1002/humu.23594DOI Listing
October 2018

Restrictive Dermopathy: Four Case Reports and Structural Skin Changes.

Acta Derm Venereol 2018 Aug;98(8):807-808

Department of Dermatology, University of Heidelberg, DE-69120 Heidelberg, Germany.

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http://dx.doi.org/10.2340/00015555-2970DOI Listing
August 2018

Integra-Dermal Regeneration Template and Split-Thickness Skin Grafting: A Therapy Approach to Correct Aplasia Cutis Congenita and Epidermolysis Bullosa in Carmi Syndrome.

Dermatol Ther (Heidelb) 2018 Jun 18;8(2):313-321. Epub 2018 May 18.

Department and Clinic of Pediatric Surgery, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

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http://dx.doi.org/10.1007/s13555-018-0237-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6002319PMC
June 2018

Deletion of a Pathogenic Mutation-Containing Exon of COL7A1 Allows Clonal Gene Editing Correction of RDEB Patient Epidermal Stem Cells.

Mol Ther Nucleic Acids 2018 Jun 31;11:68-78. Epub 2018 Jan 31.

Epithelial Biomedicine Division, Centro de Investigaciones Energéticas Medioambientales y Tecnológicas (CIEMAT), Madrid, Spain; Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz, Madrid, Spain; Centro de Investigación Biomédica en Red en Enfermedades Raras (CIBERER) U714, Madrid, Spain. Electronic address:

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http://dx.doi.org/10.1016/j.omtn.2018.01.009DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852297PMC
June 2018

Familial aortic disease and a large duplication in chromosome 16p13.1.

Mol Genet Genomic Med 2018 05 14;6(3):441-445. Epub 2018 Feb 14.

Department of Neurology, University Hospital Heidelberg, Heidelberg, Germany.

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http://dx.doi.org/10.1002/mgg3.371DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014459PMC
May 2018

Large Deletions Targeting the Triple-Helical Domain of Collagen VII Lead to Mild Acral Dominant Dystrophic Epidermolysis Bullosa.

J Invest Dermatol 2018 04 24;138(4):987-991. Epub 2017 Nov 24.

Department of Dermatology, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.jid.2017.11.014DOI Listing
April 2018

Recurrence of cervical artery dissection: An underestimated risk.

Neurology 2018 04 16;90(16):e1372-e1378. Epub 2018 Mar 16.

From the Department of Neurology (M.K., C.G.-G., P.R., W.H.), University of Heidelberg; Institute of Pathology IPH (I.H.), Heidelberg University Hospital, Germany; and Suva/Swiss National Accident Insurance Fund (T.B.), Lucerne, Switzerland.

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http://www.neurology.org/lookup/doi/10.1212/WNL.000000000000
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http://dx.doi.org/10.1212/WNL.0000000000005324DOI Listing
April 2018

Spiny keratoderma of the palms and soles - once seen, never forgotten.

J Dtsch Dermatol Ges 2017 Sep;15(9):939-941

Department of Dermatology, University Hospital Heidelberg, Heidelberg, Germany.

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http://dx.doi.org/10.1111/ddg.13313DOI Listing
September 2017

Spiny Keratoderma der Hand- und Fußflächen - einmal gesehen, nie wieder vergessen.

J Dtsch Dermatol Ges 2017 Sep;15(9):938-940

Universitätshautklinik Heidelberg, Ruprecht-Karls-Universität Heidelberg, Heidelberg.

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http://dx.doi.org/10.1111/ddg.13313_gDOI Listing
September 2017

Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans.

Am J Hum Genet 2017 Jun;100(6):926-939

Institute of Human Genetics, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, 79106 Freiburg, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2017.05.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473727PMC
June 2017

TGFBR2-dependent alterations of exosomal cargo and functions in DNA mismatch repair-deficient HCT116 colorectal cancer cells.

Cell Commun Signal 2017 04 4;15(1):14. Epub 2017 Apr 4.

Department of Applied Tumor Biology, Institute of Pathology, University Hospital Heidelberg, Im Neuenheimer Feld 224, 69120, Heidelberg, Germany.

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http://dx.doi.org/10.1186/s12964-017-0169-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379773PMC
April 2017

Collagen VII Half-Life at the Dermal-Epidermal Junction Zone: Implications for Mechanisms and Therapy of Genodermatoses.

J Invest Dermatol 2016 06 18;136(6):1116-1123. Epub 2016 Feb 18.

Department of Dermatology, Medical Center-University of Freiburg, 79104 Freiburg, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.jid.2016.02.002DOI Listing
June 2016

Increased expression of caspase-1 and interleukin-18 in peeling skin disease, and a novel mutation of corneodesmosin.

Acta Derm Venereol 2015 Nov;95(8):1019-21

Department of Dermatology, University of Münster, Von-Esmarch-Str. 58, DE-48149 Münster, Germany.

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http://dx.doi.org/10.2340/00015555-2142DOI Listing
November 2015

Molecular Consequences of the SERPINH1/HSP47 Mutation in the Dachshund Natural Model of Osteogenesis Imperfecta.

J Biol Chem 2015 Jul 24;290(29):17679-89. Epub 2015 May 24.

From the Division of Metabolism, Connective Tissue Unit, University Children's Hospital Zurich, Children's Research Center, 8032 Zurich, Switzerland,

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http://dx.doi.org/10.1074/jbc.M115.661025DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4505018PMC
July 2015

Whole-exome sequencing in patients with ichthyosis reveals modifiers associated with increased IgE levels and allergic sensitizations.

J Allergy Clin Immunol 2015 Jan 11;135(1):280-3. Epub 2014 Nov 11.

Department of Dermatology, Medical Center, University of Freiburg, Freiburg, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.jaci.2014.09.042DOI Listing
January 2015

Early venous manifestation of Ehlers-Danlos syndrome Type IV through a novel mutation in COL3A1.

Cardiovasc Pathol 2013 Nov-Dec;22(6):488-92. Epub 2013 May 17.

Clinic of Vascular Surgery, Klinikum rechts der Isar der Technischen Universitaet Muenchen, Germany.

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http://dx.doi.org/10.1016/j.carpath.2013.04.003DOI Listing
June 2014

Annular atrophic plaques on the face in a father and a son: Christianson's disease, a real entity?

Acta Derm Venereol 2014 Jan;94(1):100-1

Department of Dermatology, University Medical Center Mannheim, Heidelberg University, Theodor-Kutzer-Ufer 1-3, DE-68135 Mannheim, Germany.

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http://dx.doi.org/10.2340/00015555-1604DOI Listing
January 2014

Bilateral vertebral artery dissection, agenesis of both ICAs, and connective tissue aberrations.

Neurology 2013 Apr;80(15):1442-3

Rhine Main Neuroscience Network (rmn2), Johannes Gutenberg University Center, Department of Neurology, Mainz, Germany.

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http://dx.doi.org/10.1212/WNL.0b013e31828c2f8eDOI Listing
April 2013

ClpV recycles VipA/VipB tubules and prevents non-productive tubule formation to ensure efficient type VI protein secretion.

Mol Microbiol 2013 Mar 3;87(5):1013-28. Epub 2013 Feb 3.

Center for Molecular Biology of the University of Heidelberg and German Cancer Research Center, DKFZ-ZMBH Alliance, Universität Heidelberg, Im Neuenheimer Feld 282, 69120 Heidelberg, Germany.

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http://dx.doi.org/10.1111/mmi.12147DOI Listing
March 2013

Aloxe3 knockout mice reveal a function of epidermal lipoxygenase-3 as hepoxilin synthase and its pivotal role in barrier formation.

J Invest Dermatol 2013 Jan 26;133(1):172-80. Epub 2012 Jul 26.

Genome Modifications and Carcinogenesis, German Cancer Research Center, Heidelberg, Germany.

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http://dx.doi.org/10.1038/jid.2012.250DOI Listing
January 2013

Keratin 1 maintains skin integrity and participates in an inflammatory network in skin through interleukin-18.

J Cell Sci 2012 Nov 6;125(Pt 22):5269-79. Epub 2012 Nov 6.

Translational Centre for Regenerative Medicine and Institute of Biology, University of Leipzig, 04103 Leipzig, Germany.

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http://dx.doi.org/10.1242/jcs.116574DOI Listing
November 2012

Ichthyosis prematurity syndrome: clinical evaluation of 17 families with a rare disorder of lipid metabolism.

J Am Acad Dermatol 2012 Apr 19;66(4):606-16. Epub 2011 Aug 19.

Department of Pathology and Centre of Immune Regulation, Oslo University Hospital-Rikshospitalet and University of Oslo, Oslo, Norway.

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http://dx.doi.org/10.1016/j.jaad.2011.04.014DOI Listing
April 2012

Congenital ichthyosis in severe type II Gaucher disease with a homozygous null mutation.

Neonatology 2011 1;100(2):194-7. Epub 2011 Apr 1.

Department of Pediatrics, Klinikum Neukoelln, Berlin, Germany.

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http://dx.doi.org/10.1159/000324116DOI Listing
January 2012

[A family with dystrophic alopecia and keratosis pilaris].

J Dtsch Dermatol Ges 2011 Dec;9(12):1055-6

Universitäts-Hautklinik, Ruprecht-Karls-Universität Heidelberg Institut für Humangenetik, Ruprecht-Karls-Universität Heidelberg.

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http://dx.doi.org/10.1111/j.1610-0387.2011.07792.xDOI Listing
December 2011

Palmoplantar hyperkeratoses and hypopigmentation. Cole disease.

Acta Derm Venereol 2011 Oct;91(6):737-8

Department of Dermatology, University Medical Centre Mannheim, Heidelberg University, Theodor-Kutzer-Ufer 1-3, 68135 Mannheim, Germany.

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http://dx.doi.org/10.2340/00015555-1122DOI Listing
October 2011

Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entity.

Hum Mol Genet 2011 May 14;20(9):1811-9. Epub 2011 Feb 14.

Department of Dermatology, University Medical Center Freiburg, Hauptstr. 7, Freiburg 79104, Germany.

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http://dx.doi.org/10.1093/hmg/ddr064DOI Listing
May 2011

Bathing suit ichthyosis.

Eur J Dermatol 2010 Jul-Aug;20(4):447-50. Epub 2010 Jun 3.

Department of Dermatology, Hospital de Cascais, Av. Brigadeiro Victor Novais Gonçalves, 2755-009 Cascais, Portugal.

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http://dx.doi.org/10.1684/ejd.2010.1008DOI Listing
September 2010

Dyschromatosis ptychotropica: an unusual pigmentary disorder in a boy with epileptic encephalopathy and progressive atrophy of the central nervous system-a novel entity?

Eur J Pediatr 2010 Apr 26;169(4):495-500. Epub 2009 Aug 26.

Department of Neuropediatrics, University Medical Center Schleswig-Holstein, Kiel Campus, Arnold-Heller-Str. 3, Haus 9, 24105, Kiel, Germany.

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http://link.springer.com/10.1007/s00431-009-1046-5
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http://dx.doi.org/10.1007/s00431-009-1046-5DOI Listing
April 2010

In vitro cutaneous application of ISCOMs on human skin enhances delivery of hydrophobic model compounds through the stratum corneum.

AAPS J 2009 Dec 28;11(4):728-39. Epub 2009 Oct 28.

Department of Pharmaceutics and Analytical Chemistry, Faculty of Pharmaceutical Sciences, University of Copenhagen, Universitetsparken 2, 2100, Copenhagen, Denmark.

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http://dx.doi.org/10.1208/s12248-009-9149-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2782083PMC
December 2009

Development of an ichthyosiform phenotype in Alox12b-deficient mouse skin transplants.

J Invest Dermatol 2009 Jun 1;129(6):1429-36. Epub 2009 Jan 1.

Genome Modifications and Carcinogenesis, German Cancer Research Center, Heidelberg, Germany.

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http://dx.doi.org/10.1038/jid.2008.410DOI Listing
June 2009

Ichthyosis, follicular atrophoderma, and hypotrichosis caused by mutations in ST14 is associated with impaired profilaggrin processing.

J Invest Dermatol 2009 Apr 9;129(4):862-9. Epub 2008 Oct 9.

Division of Dermatogenetics, Cologne Center for Genomics, University of Cologne, Cologne, Germany.

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http://dx.doi.org/10.1038/jid.2008.311DOI Listing
April 2009

Restrictive dermopathy: a rare laminopathy.

Arch Gynecol Obstet 2008 Sep 10;278(3):201-8. Epub 2008 May 10.

Department of Gynecology and Obstetrics, Klinikum Offenbach, Starkenburgring 66, 63069, Offenbach, Germany.

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http://dx.doi.org/10.1007/s00404-008-0676-6DOI Listing
September 2008

Ultrastructural evidence of dermal gadolinium deposits in a patient with nephrogenic systemic fibrosis and end-stage renal disease.

Clin J Am Soc Nephrol 2008 Jul 2;3(4):968-75. Epub 2008 Apr 2.

Klinik und Poliklinik für Innere, Medizin II-Nephrologie, University of Regensburg, Franz-Josef-Strauss-Allee 11, 93053 Regensburg, Germany.

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http://dx.doi.org/10.2215/CJN.00100108DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2440263PMC
July 2008

Erythema elevatum diutinum with unusual clinical appearance.

J Dtsch Dermatol Ges 2008 Apr 11;6(4):303-5. Epub 2008 Feb 11.

University Dermatology Clinic, Heidelberg, Germany.

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http://dx.doi.org/10.1111/j.1610-0387.2008.06589.xDOI Listing
April 2008

Highly variable cutis laxa resulting from a dominant splicing mutation of the elastin gene.

Am J Med Genet A 2008 Apr;146A(8):977-83

Institute of Human Genetics, Charité, Campus Virchow-Klinikum, Berlin, Germany.

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http://dx.doi.org/10.1002/ajmg.a.32242DOI Listing
April 2008

Pathology of the large intestine in patients with vascular type Ehlers-Danlos syndrome.

Virchows Arch 2007 Jun 9;450(6):713-7. Epub 2007 May 9.

Institute of Pathology, University of Heidelberg, INF 220, 69120 Heidelberg, Germany.

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http://dx.doi.org/10.1007/s00428-007-0415-6DOI Listing
June 2007

Hyalinosis cutis et mucosae.

J Dtsch Dermatol Ges 2007 May;5(5):401-5

Department of Dermatology, University of Heidelberg, Germany.

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http://dx.doi.org/10.1111/j.1610-0387.2007.06284.xDOI Listing
May 2007

12R-lipoxygenase deficiency disrupts epidermal barrier function.

J Cell Biol 2007 Apr 2;177(1):173-82. Epub 2007 Apr 2.

Section Eicosanoids and Tumor Development, German Cancer Research Center, D-69120 Heidelberg, Germany.

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http://dx.doi.org/10.1083/jcb.200612116DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064121PMC
April 2007

Junctional basement membrane anomalies of skin and mucosa in lipoid proteinosis (hyalinosis cutis et mucosae).

J Dermatol Sci 2007 Mar 15;45(3):175-85. Epub 2006 Dec 15.

German Cancer Research Center, Division Genetics of Skin Cancer, Heidelberg, Germany.

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http://dx.doi.org/10.1016/j.jdermsci.2006.11.010DOI Listing
March 2007

Familial cervical artery dissections: clinical, morphologic, and genetic studies.

Stroke 2006 Dec 19;37(12):2924-9. Epub 2006 Oct 19.

Department of Neurology, Sanatorio Allende, Hipólito Irigoyen 384, CP 5000, Córdoba, Argentine.

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http://dx.doi.org/10.1161/01.STR.0000248916.52976.49DOI Listing
December 2006

Images in vascular medicine. Pseudoxanthoma elasticum: under-recognized cause of early onset peripheral arterial disease?

Vasc Med 2006 Nov;11(4):266-7

Klinikum Karlsbad-Langensteinbach, Teaching Hospital of the Ruprecht-Karls-University Heidelberg, D-76307 Karlsbad, Germany.

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http://dx.doi.org/10.1177/1358863x06075186DOI Listing
November 2006

Vascular anomalies in lipoid proteinosis (hyalinosis cutis et mucosae): basement membrane components and ultrastructure.

J Dermatol Sci 2006 Jun 21;42(3):231-9. Epub 2006 Feb 21.

German Cancer Research Center, Division Carcinogenesis and Differentiation, Heidelberg, Germany.

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http://dx.doi.org/10.1016/j.jdermsci.2006.01.004DOI Listing
June 2006

A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis.

Hum Mol Genet 2006 Apr 27;15(7):1133-41. Epub 2006 Feb 27.

Department of Dermatology, University of Cologne, 50924 Köln, Germany.

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http://academic.oup.com/hmg/article/15/7/1133/715392/A-human
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http://dx.doi.org/10.1093/hmg/ddl028DOI Listing
April 2006

[Ehlers-Danlos syndrome--20 years experience with diagnosis and classification at the university skin clinic of Heidelberg].

J Dtsch Dermatol Ges 2006 Apr;4(4):308-18

Department of Dermatology, University of Heidelberg, Germany.

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http://dx.doi.org/10.1111/j.1610-0387.2006.05958.xDOI Listing
April 2006

Novel autosomal recessive progressive hyperpigmentation syndrome.

Am J Med Genet A 2005 Jun;135(2):195-9

Institute of Human Genetics, Friedrich-Alexander University of Erlangen-Nuremberg, Germany.

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http://dx.doi.org/10.1002/ajmg.a.30668DOI Listing
June 2005

Ullrich congenital muscular dystrophy: connective tissue abnormalities in the skin support overlap with Ehlers-Danlos syndromes.

Am J Med Genet A 2005 Jan;132A(3):296-301

Division of Neurology, The Children's Hospital of Philadelphia, and University of Pennsylvania Medical School, Philadelphia, Pennsylvania 19104, USA.

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http://dx.doi.org/10.1002/ajmg.a.30443DOI Listing
January 2005

Different types of connective tissue alterations associated with cervical artery dissections.

Acta Neuropathol 2004 Jun 6;107(6):509-14. Epub 2004 Apr 6.

Department of Dermatology, University of Heidelberg, Heidelberg, Germany.

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http://dx.doi.org/10.1007/s00401-004-0839-xDOI Listing
June 2004