Pęcherzowe oddzielanie się naskórka (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Pęcherzowe oddzielanie się naskórka" in Polish language version.

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7doi.org

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6nih.gov

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4worldcat.org

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2nature.com

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archive.ph

S.S. Chavanas S.S. i inni, Splicing Modulation of Integrin (β4 Pre-mRNA) Carrying a Branch Point Mutation Underlies Epidermolysis Bullosa with Pyloric Atresia Undergoing Spontaneous Amelioration With Ageing, „Human Molecular Genetics”, 8 (11), 1999, s. 2097–2105, DOI: 10.1093/hmg/8.11.2097, ISSN 0964-6906, PMID: 10484780 [dostęp 2017-01-03] [zarchiwizowane z adresu 2017-01-04] (ang.).

doi.org

dx.doi.org

KanaK. Yasukawa KanaK. i inni, Dominant and Recessive Compound Heterozygous Mutations in Epidermolysis Bullosa Simplex Demonstrate the Role of the Stutter Region in Keratin Intermediate Filament Assembly, „Journal of Biological Chemistry”, 26, 2002, s. 23670–23674, DOI: 10.1074/jbc.M200974200, ISSN 0021-9258, PMID: 11973334 [dostęp 2017-01-03] (ang.).
Jo-DavidJ.D. Fine Jo-DavidJ.D. i inni, The classification of inherited epidermolysis bullosa (EB): report of the Third International Consensus Meeting on diagnosis and classification of EB, „J. Am. Acad. Derm.”, 58 (6), 2008, s. 931–950, DOI: 10.1016/j.jaad.2008.02.004, PMID: 18374450 .
ShoshanaS. Hacham-Zadeh ShoshanaS. i inni, Epidermolysis bullosa herpetiformis Dowling-Meara in a large family, „J. Am. Acad. Derm.”, 18 (4 Pt 1), 1988, s. 702–706, DOI: 10.1016/s0190-9622(88)70093-6, PMID: 3372762 .
F.J.D.F.J.D. Smith F.J.D.F.J.D. i inni, Plectin deficiency results in muscular dystrophy with epidermolysis bullosa, „Nature Genetics”, 4, 1996, s. 450–457, DOI: 10.1038/ng0896-450 [dostęp 2017-01-03] (ang.).
FrédériqueF. Vidal FrédériqueF. i inni, Integrin β4 mutations associated with junctional epidermolysis bullosa with pyloric atresia, „Nature Genetics”, 10, 1995, s. 229–234, DOI: 10.1038/ng0695-229 [dostęp 2017-01-03] (ang.).
S.S. Chavanas S.S. i inni, Splicing Modulation of Integrin (β4 Pre-mRNA) Carrying a Branch Point Mutation Underlies Epidermolysis Bullosa with Pyloric Atresia Undergoing Spontaneous Amelioration With Ageing, „Human Molecular Genetics”, 8 (11), 1999, s. 2097–2105, DOI: 10.1093/hmg/8.11.2097, ISSN 0964-6906, PMID: 10484780 [dostęp 2017-01-03] [zarchiwizowane z adresu 2017-01-04] (ang.).
J.J. Diedrichson J.J., D.D. Talanow D.D., A.A. Safi A.A., [Epidermolysis bullosa dystrophica (Hallopeau-Siemens syndrome) of the hand -- surgical strategy and results], „Handchirurgie, Mikrochirurgie, Plastische Chirurgie: Organ Der Deutschsprachigen Arbeitsgemeinschaft Fur Handchirurgie: Organ Der Deutschsprachigen Arbeitsgemeinschaft Fur Mikrochirurgie Der Peripheren Nerven Und Gefasse: Organ Der V...”, 37 (5), 2005, s. 316–322, DOI: 10.1055/s-2005-872849, ISSN 0722-1819, PMID: 16287016 [dostęp 2017-01-03] .

jbc.org

KanaK. Yasukawa KanaK. i inni, Dominant and Recessive Compound Heterozygous Mutations in Epidermolysis Bullosa Simplex Demonstrate the Role of the Stutter Region in Keratin Intermediate Filament Assembly, „Journal of Biological Chemistry”, 26, 2002, s. 23670–23674, DOI: 10.1074/jbc.M200974200, ISSN 0021-9258, PMID: 11973334 [dostęp 2017-01-03] (ang.).

nature.com

F.J.D.F.J.D. Smith F.J.D.F.J.D. i inni, Plectin deficiency results in muscular dystrophy with epidermolysis bullosa, „Nature Genetics”, 4, 1996, s. 450–457, DOI: 10.1038/ng0896-450 [dostęp 2017-01-03] (ang.).
FrédériqueF. Vidal FrédériqueF. i inni, Integrin β4 mutations associated with junctional epidermolysis bullosa with pyloric atresia, „Nature Genetics”, 10, 1995, s. 229–234, DOI: 10.1038/ng0695-229 [dostęp 2017-01-03] (ang.).

nih.gov

ncbi.nlm.nih.gov

KanaK. Yasukawa KanaK. i inni, Dominant and Recessive Compound Heterozygous Mutations in Epidermolysis Bullosa Simplex Demonstrate the Role of the Stutter Region in Keratin Intermediate Filament Assembly, „Journal of Biological Chemistry”, 26, 2002, s. 23670–23674, DOI: 10.1074/jbc.M200974200, ISSN 0021-9258, PMID: 11973334 [dostęp 2017-01-03] (ang.).
Jo-DavidJ.D. Fine Jo-DavidJ.D. i inni, The classification of inherited epidermolysis bullosa (EB): report of the Third International Consensus Meeting on diagnosis and classification of EB, „J. Am. Acad. Derm.”, 58 (6), 2008, s. 931–950, DOI: 10.1016/j.jaad.2008.02.004, PMID: 18374450 .
ShoshanaS. Hacham-Zadeh ShoshanaS. i inni, Epidermolysis bullosa herpetiformis Dowling-Meara in a large family, „J. Am. Acad. Derm.”, 18 (4 Pt 1), 1988, s. 702–706, DOI: 10.1016/s0190-9622(88)70093-6, PMID: 3372762 .
S.S. Chavanas S.S. i inni, Splicing Modulation of Integrin (β4 Pre-mRNA) Carrying a Branch Point Mutation Underlies Epidermolysis Bullosa with Pyloric Atresia Undergoing Spontaneous Amelioration With Ageing, „Human Molecular Genetics”, 8 (11), 1999, s. 2097–2105, DOI: 10.1093/hmg/8.11.2097, ISSN 0964-6906, PMID: 10484780 [dostęp 2017-01-03] [zarchiwizowane z adresu 2017-01-04] (ang.).
C.A.C.A. Oakley C.A.C.A. i inni, The Cockayne-Touraine type of dominant dystrophic epidermolysis bullosa--ultrastructural similarities to the Pasini variant, „Acta Dermato-Venereologica”, 64 (3), 1984, s. 253–256, ISSN 0001-5555, PMID: 6204490 [dostęp 2017-01-03] .
J.J. Diedrichson J.J., D.D. Talanow D.D., A.A. Safi A.A., [Epidermolysis bullosa dystrophica (Hallopeau-Siemens syndrome) of the hand -- surgical strategy and results], „Handchirurgie, Mikrochirurgie, Plastische Chirurgie: Organ Der Deutschsprachigen Arbeitsgemeinschaft Fur Handchirurgie: Organ Der Deutschsprachigen Arbeitsgemeinschaft Fur Mikrochirurgie Der Peripheren Nerven Und Gefasse: Organ Der V...”, 37 (5), 2005, s. 316–322, DOI: 10.1055/s-2005-872849, ISSN 0722-1819, PMID: 16287016 [dostęp 2017-01-03] .

oxfordjournals.org

hmg.oxfordjournals.org

S.S. Chavanas S.S. i inni, Splicing Modulation of Integrin (β4 Pre-mRNA) Carrying a Branch Point Mutation Underlies Epidermolysis Bullosa with Pyloric Atresia Undergoing Spontaneous Amelioration With Ageing, „Human Molecular Genetics”, 8 (11), 1999, s. 2097–2105, DOI: 10.1093/hmg/8.11.2097, ISSN 0964-6906, PMID: 10484780 [dostęp 2017-01-03] [zarchiwizowane z adresu 2017-01-04] (ang.).

worldcat.org

KanaK. Yasukawa KanaK. i inni, Dominant and Recessive Compound Heterozygous Mutations in Epidermolysis Bullosa Simplex Demonstrate the Role of the Stutter Region in Keratin Intermediate Filament Assembly, „Journal of Biological Chemistry”, 26, 2002, s. 23670–23674, DOI: 10.1074/jbc.M200974200, ISSN 0021-9258, PMID: 11973334 [dostęp 2017-01-03] (ang.).
S.S. Chavanas S.S. i inni, Splicing Modulation of Integrin (β4 Pre-mRNA) Carrying a Branch Point Mutation Underlies Epidermolysis Bullosa with Pyloric Atresia Undergoing Spontaneous Amelioration With Ageing, „Human Molecular Genetics”, 8 (11), 1999, s. 2097–2105, DOI: 10.1093/hmg/8.11.2097, ISSN 0964-6906, PMID: 10484780 [dostęp 2017-01-03] [zarchiwizowane z adresu 2017-01-04] (ang.).
C.A.C.A. Oakley C.A.C.A. i inni, The Cockayne-Touraine type of dominant dystrophic epidermolysis bullosa--ultrastructural similarities to the Pasini variant, „Acta Dermato-Venereologica”, 64 (3), 1984, s. 253–256, ISSN 0001-5555, PMID: 6204490 [dostęp 2017-01-03] .
J.J. Diedrichson J.J., D.D. Talanow D.D., A.A. Safi A.A., [Epidermolysis bullosa dystrophica (Hallopeau-Siemens syndrome) of the hand -- surgical strategy and results], „Handchirurgie, Mikrochirurgie, Plastische Chirurgie: Organ Der Deutschsprachigen Arbeitsgemeinschaft Fur Handchirurgie: Organ Der Deutschsprachigen Arbeitsgemeinschaft Fur Mikrochirurgie Der Peripheren Nerven Und Gefasse: Organ Der V...”, 37 (5), 2005, s. 316–322, DOI: 10.1055/s-2005-872849, ISSN 0722-1819, PMID: 16287016 [dostęp 2017-01-03] .