Генерализована еластолиза (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Генерализована еластолиза" in Serbian language version.

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30doi.org

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9nih.gov

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6worldcat.org

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3semanticscholar.org

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2archive.org

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1medscape.com

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archive.org

Hill, V.A.; Seymour, C.A.; Mortimer, P.S. (март 2000). „Penicillamine-induced elastosis perforans serpiginosa and cutis laxa in Wilson's disease”. British Journal of Dermatology. 142 (3): 560—1. PMID 10777259. S2CID 72673405. doi:10.1046/j.1365-2133.2000.03379.x. .
Anderson, Carol E.; Finklestein, Jerry Z.; Nussbaum, Eliezer; Larson, Eunice J.; Halpern, Roy; Uitto, Jouni; Tanaka, Kouichi R. (август 1984). „Association of hemolytic anemia and early-onset pulmonary emphysema in three siblings”. J Pediatr. 105 (2): 247—51. PMID 6747755. doi:10.1016/s0022-3476(84)80121-3. .

doi.org

dx.doi.org

Bayart, Cheryl B.; Brandling-Bennett, Heather A. (2018), Congenital and Hereditary Disorders of the Skin, Elsevier, стр. 1475—1494.e1, ISBN 978-0-323-40139-5, Приступљено 2024-01-20
Uitto, Jouni (2013), Heritable Diseases Affecting the Elastic Fibers, Elsevier, стр. 1—30, ISBN 978-0-12-383834-6, Приступљено 2024-01-20
Kumar, Piyush; Savant, Sushil S; Das, Anupam (2016). „Generalized acquired cutis laxa type 1: a case report and brief review of literature”. Dermatology Online Journal. 22 (3). ISSN 1087-2108. doi:10.5070/d3223030369.
Redmond, John Mark (2018), Genetic Basis of Aortic Disease, Elsevier, стр. 91—100, Приступљено 2024-01-20
Paller, Amy S.; Mancini, Anthony J. (2016), Hereditary Disorders of the Dermis, Elsevier, стр. 119—135.e6, Приступљено 2024-01-20
Hu, Qirui; Reymond, Jean-Louis; Pinel, Nicole; Zabot, Marie-Therese; Urban, Zsolt (2006). „Inflammatory Destruction of Elastic Fibers in Acquired Cutis Laxa Is Associated with Missense Alleles in the Elastin and Fibulin-5 Genes”. Journal of Investigative Dermatology. 126 (2): 283—290. ISSN 0022-202X. doi:10.1038/sj.jid.5700047.
Paller, Amy S.; Mancini, Anthony J. (2011), Hereditary Disorders of the Dermis, Elsevier, стр. 115—129, Приступљено 2024-01-20
Urban, Zsolt; Hucthagowder, Vishwanathan; Schürmann, Nura; Todorovic, Vesna; Zilberberg, Lior; Choi, Jiwon; Sens, Carla; Brown, Chester W.; Clark, Robin D. (2009). „Mutations in LTBP4 Cause a Syndrome of Impaired Pulmonary, Gastrointestinal, Genitourinary, Musculoskeletal, and Dermal Development”. The American Journal of Human Genetics. 85 (5): 593—605. ISSN 0002-9297. doi:10.1016/j.ajhg.2009.09.013.
Pope, F.M. (2001), Cutis Laxa, Elsevier, стр. 497—499, Приступљено 2024-01-20
Morrell, Dean S.; Burkhart, Craig N.; Siegel, Dawn (2008), Selected Hereditary Diseases, Elsevier, стр. 477—501, Приступљено 2024-01-20
Vanakker, Olivier; Callewaert, Bert; Malfait, Fransiska; Coucke, Paul (2015-08-24). „The Genetics of Soft Connective Tissue Disorders”. Annual Review of Genomics and Human Genetics. 16 (1): 229—255. ISSN 1527-8204. doi:10.1146/annurev-genom-090314-050039.
Callewaert, Bert; Renard, Marjolijn; Hucthagowder, Vishwanathan; Albrecht, Beate; Hausser, Ingrid; Blair, Edward; Dias, Cristina; Albino, Alice; Wachi, Hiroshi (2011). „New insights into the pathogenesis of autosomal‐dominant cutis laxa with report of fiveELNmutations”. Human Mutation. 32 (4): 445—455. ISSN 1059-7794. doi:10.1002/humu.21462.
Morava, E; Lefeber, D J; Urban, Z; de Meirleir, L; Meinecke, P; Gillessen Kaesbach, G; Sykut-Cegielska, J; Adamowicz, M; Salafsky, I (2007-10-31). „Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation”. European Journal of Human Genetics. 16 (1): 28—35. ISSN 1018-4813. doi:10.1038/sj.ejhg.5201947.
Monahan, Timothy P.; Cohen, Bernard A.; Siegfried, Elaine C. (2005), Congenital and Hereditary Disorders of the Skin, Elsevier, стр. 1483—1502, ISBN 978-0-7216-9347-7, Приступљено 2024-01-20
Gardeitchik, T.; Morava, E. (2013), Cutis Laxa, Elsevier, стр. 254—257, Приступљено 2024-01-20

doi.org

Kumar, Piyush; Savant, Sushil S; Das, Anupam (2016). „Generalized acquired cutis laxa type 1: a case report and brief review of literature”. Dermatology Online Journal. 22 (3). ISSN 1087-2108. doi:10.5070/d3223030369.
Hu, Qirui; Reymond, Jean-Louis; Pinel, Nicole; Zabot, Marie-Therese; Urban, Zsolt (2006). „Inflammatory Destruction of Elastic Fibers in Acquired Cutis Laxa Is Associated with Missense Alleles in the Elastin and Fibulin-5 Genes”. Journal of Investigative Dermatology. 126 (2): 283—290. ISSN 0022-202X. doi:10.1038/sj.jid.5700047.
Urban, Zsolt; Hucthagowder, Vishwanathan; Schürmann, Nura; Todorovic, Vesna; Zilberberg, Lior; Choi, Jiwon; Sens, Carla; Brown, Chester W.; Clark, Robin D. (2009). „Mutations in LTBP4 Cause a Syndrome of Impaired Pulmonary, Gastrointestinal, Genitourinary, Musculoskeletal, and Dermal Development”. The American Journal of Human Genetics. 85 (5): 593—605. ISSN 0002-9297. doi:10.1016/j.ajhg.2009.09.013.
Randle HW, Muller S (јун 1983). „Generalized elastolysis associated with systemic lupus erythematosus”. Journal of the American Academy of Dermatology. 8 (6): 869—73. PMID 6345611. doi:10.1016/S0190-9622(83)80019-X. .
Vanakker, Olivier; Callewaert, Bert; Malfait, Fransiska; Coucke, Paul (2015-08-24). „The Genetics of Soft Connective Tissue Disorders”. Annual Review of Genomics and Human Genetics. 16 (1): 229—255. ISSN 1527-8204. doi:10.1146/annurev-genom-090314-050039.
Callewaert, Bert; Renard, Marjolijn; Hucthagowder, Vishwanathan; Albrecht, Beate; Hausser, Ingrid; Blair, Edward; Dias, Cristina; Albino, Alice; Wachi, Hiroshi (2011). „New insights into the pathogenesis of autosomal‐dominant cutis laxa with report of fiveELNmutations”. Human Mutation. 32 (4): 445—455. ISSN 1059-7794. doi:10.1002/humu.21462.
Morava, E; Lefeber, D J; Urban, Z; de Meirleir, L; Meinecke, P; Gillessen Kaesbach, G; Sykut-Cegielska, J; Adamowicz, M; Salafsky, I (2007-10-31). „Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation”. European Journal of Human Genetics. 16 (1): 28—35. ISSN 1018-4813. doi:10.1038/sj.ejhg.5201947.
Nozaki, F.; Kusunoki, T.; Okamoto, N.; Yamamoto, Y.; Miya, F.; Tsunoda, T.; Kosaki, K.; Kumada, T.; Shibata, M.; Fujii, T. (август 2016). „ALDH18A1-related cutis laxa syndrome with cyclic vomiting”. Brain Dev. 38 (7): 678—84. PMID 26829900. S2CID 206315735. doi:10.1016/j.braindev.2016.01.003. .
Hill, V.A.; Seymour, C.A.; Mortimer, P.S. (март 2000). „Penicillamine-induced elastosis perforans serpiginosa and cutis laxa in Wilson's disease”. British Journal of Dermatology. 142 (3): 560—1. PMID 10777259. S2CID 72673405. doi:10.1046/j.1365-2133.2000.03379.x. .
New, H. D.; Callen, J. P. (март 2011). „Generalized acquired cutis laxa associated with multiple myeloma with biphenotypic IgG-? and IgA-? gammopathy following treatment of a nodal plasmacytoma”. Arch Dermatol. 147 (3): 323—8. PMID 21422340. doi:10.1001/archdermatol.2011.26. .
o'Malley, John T.; d'Agati, Vivette D.; Sherman, William H.; Grossman, Marc E. (2014). „Acquired Cutis Laxa Associated with Heavy Chain Deposition Disease Involving Dermal Elastic Fibers”. JAMA Dermatology. 150 (11): 1192—1196. PMID 25133950. doi:10.1001/jamadermatol.2014.725.
Koklu, Esad; Gunes, Tamer; Ozturk, Mehmet Adnan; Akcakus, Mustafa; Buyukkayhan, Derya; Kurtoglu, Selim (2007). „Cutis laxa associated with central hypothyroidism owing to isolated thyrotropin deficiency in a newborn”. Pediatr Dermatol. 24 (5): 525—8. PMID 17958802. S2CID 21036294. doi:10.1111/j.1525-1470.2007.00509.x.
Anderson, Carol E.; Finklestein, Jerry Z.; Nussbaum, Eliezer; Larson, Eunice J.; Halpern, Roy; Uitto, Jouni; Tanaka, Kouichi R. (август 1984). „Association of hemolytic anemia and early-onset pulmonary emphysema in three siblings”. J Pediatr. 105 (2): 247—51. PMID 6747755. doi:10.1016/s0022-3476(84)80121-3. .
Alehossein, Mehdi; Pourgholami, Masoud; Kamrani, Kamyar; Soltani, Mohammad; Yazdi, Afshin; Salamati, Payman (јун 2013). „Radiologic findings in cutis laxa syndrome and unusual association with hypertrophic pyloric stenosis”. Iran J Radiol. 10 (2): 94—8. PMC 3767021 . PMID 24046787. doi:10.5812/iranjradiol.4064. .
Bharadwaj, Shishira; Shrestha, Prakash; Gohel, Tushar D.; Singh, Maninder (2014). „Cutis laxa presenting as recurrent ileus”. Gastroenterology Report. 4 (1): 77—79. PMC 4760055 . PMID 25008264. doi:10.1093/gastro/gou045.

medscape.com

emedicine.medscape.com

„Cutis Laxa (Elastolysis): Practice Essentials, Pathophysiology, Epidemiology”. emedicine.medscape.com. 2022-03-04.

nih.gov

ncbi.nlm.nih.gov

Randle HW, Muller S (јун 1983). „Generalized elastolysis associated with systemic lupus erythematosus”. Journal of the American Academy of Dermatology. 8 (6): 869—73. PMID 6345611. doi:10.1016/S0190-9622(83)80019-X. .
Nozaki, F.; Kusunoki, T.; Okamoto, N.; Yamamoto, Y.; Miya, F.; Tsunoda, T.; Kosaki, K.; Kumada, T.; Shibata, M.; Fujii, T. (август 2016). „ALDH18A1-related cutis laxa syndrome with cyclic vomiting”. Brain Dev. 38 (7): 678—84. PMID 26829900. S2CID 206315735. doi:10.1016/j.braindev.2016.01.003. .
Hill, V.A.; Seymour, C.A.; Mortimer, P.S. (март 2000). „Penicillamine-induced elastosis perforans serpiginosa and cutis laxa in Wilson's disease”. British Journal of Dermatology. 142 (3): 560—1. PMID 10777259. S2CID 72673405. doi:10.1046/j.1365-2133.2000.03379.x. .
New, H. D.; Callen, J. P. (март 2011). „Generalized acquired cutis laxa associated with multiple myeloma with biphenotypic IgG-? and IgA-? gammopathy following treatment of a nodal plasmacytoma”. Arch Dermatol. 147 (3): 323—8. PMID 21422340. doi:10.1001/archdermatol.2011.26. .
o'Malley, John T.; d'Agati, Vivette D.; Sherman, William H.; Grossman, Marc E. (2014). „Acquired Cutis Laxa Associated with Heavy Chain Deposition Disease Involving Dermal Elastic Fibers”. JAMA Dermatology. 150 (11): 1192—1196. PMID 25133950. doi:10.1001/jamadermatol.2014.725.
Koklu, Esad; Gunes, Tamer; Ozturk, Mehmet Adnan; Akcakus, Mustafa; Buyukkayhan, Derya; Kurtoglu, Selim (2007). „Cutis laxa associated with central hypothyroidism owing to isolated thyrotropin deficiency in a newborn”. Pediatr Dermatol. 24 (5): 525—8. PMID 17958802. S2CID 21036294. doi:10.1111/j.1525-1470.2007.00509.x.
Anderson, Carol E.; Finklestein, Jerry Z.; Nussbaum, Eliezer; Larson, Eunice J.; Halpern, Roy; Uitto, Jouni; Tanaka, Kouichi R. (август 1984). „Association of hemolytic anemia and early-onset pulmonary emphysema in three siblings”. J Pediatr. 105 (2): 247—51. PMID 6747755. doi:10.1016/s0022-3476(84)80121-3. .
Alehossein, Mehdi; Pourgholami, Masoud; Kamrani, Kamyar; Soltani, Mohammad; Yazdi, Afshin; Salamati, Payman (јун 2013). „Radiologic findings in cutis laxa syndrome and unusual association with hypertrophic pyloric stenosis”. Iran J Radiol. 10 (2): 94—8. PMC 3767021 . PMID 24046787. doi:10.5812/iranjradiol.4064. .
Bharadwaj, Shishira; Shrestha, Prakash; Gohel, Tushar D.; Singh, Maninder (2014). „Cutis laxa presenting as recurrent ileus”. Gastroenterology Report. 4 (1): 77—79. PMC 4760055 . PMID 25008264. doi:10.1093/gastro/gou045.

semanticscholar.org

api.semanticscholar.org

Nozaki, F.; Kusunoki, T.; Okamoto, N.; Yamamoto, Y.; Miya, F.; Tsunoda, T.; Kosaki, K.; Kumada, T.; Shibata, M.; Fujii, T. (август 2016). „ALDH18A1-related cutis laxa syndrome with cyclic vomiting”. Brain Dev. 38 (7): 678—84. PMID 26829900. S2CID 206315735. doi:10.1016/j.braindev.2016.01.003. .
Hill, V.A.; Seymour, C.A.; Mortimer, P.S. (март 2000). „Penicillamine-induced elastosis perforans serpiginosa and cutis laxa in Wilson's disease”. British Journal of Dermatology. 142 (3): 560—1. PMID 10777259. S2CID 72673405. doi:10.1046/j.1365-2133.2000.03379.x. .
Koklu, Esad; Gunes, Tamer; Ozturk, Mehmet Adnan; Akcakus, Mustafa; Buyukkayhan, Derya; Kurtoglu, Selim (2007). „Cutis laxa associated with central hypothyroidism owing to isolated thyrotropin deficiency in a newborn”. Pediatr Dermatol. 24 (5): 525—8. PMID 17958802. S2CID 21036294. doi:10.1111/j.1525-1470.2007.00509.x.

worldcat.org

Kumar, Piyush; Savant, Sushil S; Das, Anupam (2016). „Generalized acquired cutis laxa type 1: a case report and brief review of literature”. Dermatology Online Journal. 22 (3). ISSN 1087-2108. doi:10.5070/d3223030369.
Hu, Qirui; Reymond, Jean-Louis; Pinel, Nicole; Zabot, Marie-Therese; Urban, Zsolt (2006). „Inflammatory Destruction of Elastic Fibers in Acquired Cutis Laxa Is Associated with Missense Alleles in the Elastin and Fibulin-5 Genes”. Journal of Investigative Dermatology. 126 (2): 283—290. ISSN 0022-202X. doi:10.1038/sj.jid.5700047.
Urban, Zsolt; Hucthagowder, Vishwanathan; Schürmann, Nura; Todorovic, Vesna; Zilberberg, Lior; Choi, Jiwon; Sens, Carla; Brown, Chester W.; Clark, Robin D. (2009). „Mutations in LTBP4 Cause a Syndrome of Impaired Pulmonary, Gastrointestinal, Genitourinary, Musculoskeletal, and Dermal Development”. The American Journal of Human Genetics. 85 (5): 593—605. ISSN 0002-9297. doi:10.1016/j.ajhg.2009.09.013.
Vanakker, Olivier; Callewaert, Bert; Malfait, Fransiska; Coucke, Paul (2015-08-24). „The Genetics of Soft Connective Tissue Disorders”. Annual Review of Genomics and Human Genetics. 16 (1): 229—255. ISSN 1527-8204. doi:10.1146/annurev-genom-090314-050039.
Callewaert, Bert; Renard, Marjolijn; Hucthagowder, Vishwanathan; Albrecht, Beate; Hausser, Ingrid; Blair, Edward; Dias, Cristina; Albino, Alice; Wachi, Hiroshi (2011). „New insights into the pathogenesis of autosomal‐dominant cutis laxa with report of fiveELNmutations”. Human Mutation. 32 (4): 445—455. ISSN 1059-7794. doi:10.1002/humu.21462.
Morava, E; Lefeber, D J; Urban, Z; de Meirleir, L; Meinecke, P; Gillessen Kaesbach, G; Sykut-Cegielska, J; Adamowicz, M; Salafsky, I (2007-10-31). „Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation”. European Journal of Human Genetics. 16 (1): 28—35. ISSN 1018-4813. doi:10.1038/sj.ejhg.5201947.