Zespół Ehlersa-Danlosa (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Zespół Ehlersa-Danlosa" in Polish language version.

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17doi.org

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17nih.gov

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2univ-paris5.fr

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2ehlers-danlos.com.pl

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1medicinaneisecoli.it

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1archive.org

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archive.org

Tschernogubow, Über einen Fall von Cutis laxa, „Monatshefte für praktische Dermatologie”, 76 (14), 1892, s. 76 [dostęp 2019-08-10] .

doi.org

dx.doi.org

Peter H.P.H. Byers Peter H.P.H. i inni, Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome, „American Journal of Medical Genetics. Part C, Seminars in Medical Genetics”, 175 (1), 2017, s. 40–47, DOI: 10.1002/ajmg.c.31553, PMID: 28306228 .
E.L.E.L. Ehlers E.L.E.L., Cutis laxa. Neigung zu Haemorrhagien in der Haut, Lockering mehrerer Artikulationen, „Dermatologische Zeitschrift”, 8 (2), 1901, s. 173-174, DOI: 10.1159/000241857 [dostęp 2019-08-10] .
A.P.A.P. Barabas A.P.A.P., Heterogeneity of the Ehlers-Danlos syndrome: description of three clinical types and a hypothesis to explain the basic defect(s), „British Medical Journal”, 2 (5552), 1967, s. 612–613, DOI: 10.1136/bmj.2.5552.612, PMID: 6025600, PMCID: PMC1842124 .
P.P. Beighton P.P. i inni, International Nosology of Heritable Disorders of Connective Tissue, Berlin, 1986, „American Journal of Medical Genetics”, 29 (3), 1988, s. 581–594, DOI: 10.1002/ajmg.1320290316, PMID: 3287925 .
P.P. Beighton P.P. i inni, Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK), „American Journal of Medical Genetics”, 77 (1), 1999, s. 31–37, DOI: 10.1002/(SICI)1096-8628(19980428)77:1<31::AID-AJMG8>3.0.CO;2-O, PMID: 9557891 .
FransiskaF. Malfait FransiskaF. i inni, The 2017 international classification of the Ehlers-Danlos syndromes, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175 (C), 2017, DOI: 10.1002/ajmg.c.31552, PMID: 28306229 .
Patrick R.P.R. Blackburn Patrick R.P.R., Bi-allelic Alterations in AEBP1 Lead to Defective Collagen Assembly and Connective Tissue Structure Resulting in a Variant of Ehlers-Danlos Syndrome, „The American Journal of Human Genetics”, 102 (4), 2018, s. 696-705, DOI: 10.1016/j.ajhg.2018.02.018, PMID: 29606302, PMCID: PMC5985336 .
P.P. Beighton P.P., Hypermobility scoring, „British Journal of Rheumatology”, 27 (2), 1988, s. 163, DOI: 10.1093/rheumatology/27.2.163, PMID: 3365538 .
Dominique P.D.P. Germain Dominique P.D.P., Ehlers-Danlos syndrome type IV, „Orphanet Journal of Rare Diseases”, 2, 2007, s. 32, DOI: 10.1186/1750-1172-2-32, PMID: 17640391, PMCID: PMC1971255 .
Fraser C.F.C. Henderson Fraser C.F.C., Neurological and spinal manifestations of the Ehlers-Danlos syndromes, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175 (1), 2017, s. 195-211, DOI: 10.1002/ajmg.c.31549, PMID: 28220607 .
William B.W.B. Ericson William B.W.B., jr., RogerR. Wolman RogerR., Orthopaedic Management of the Ehlers–Danlos Syndromes, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175 (1), 2017, s. 188–194, DOI: 10.1002/ajmg.c.31551, PMID: 28192621 .
AsmaA. Fikree AsmaA., Gastrointestinal involvement in the Ehlers–Danlos syndromes, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175 (1), 2017, s. 181-187, DOI: 10.1002/ajmg.c.31546, PMID: 28186368 .
AlanA. Hakim AlanA., Cardiovascular autonomic dysfunction in Ehlers–Danlos syndrome—Hypermobile type, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175 (1), 2017, s. 168-174, DOI: 10.1002/ajmg.c.31543, PMID: 28160388 .
AlanA. Hakim AlanA., Chronic fatigue in Ehlers–Danlos syndrome—Hypermobile type, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175 (1), 2017, s. 175-180, DOI: 10.1002/ajmg.c.31542, PMID: 28186393 .
Suranjith L.S.L. Seneviratne Suranjith L.S.L., AnneA. Maitland AnneA., LawrenceL. Afrin LawrenceL., Mast cell disorders in Ehlers–Danlos syndrome, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175C (1), 2017, s. 226-236, DOI: 10.1002/ajmg.c.31555, PMID: 28261938 .
JohnJ. Mitakides JohnJ., Oral and mandibular manifestations in the Ehlers–Danlos syndromes, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175 (1), 2017, s. 220-225, DOI: 10.1002/ajmg.c.31541, PMID: 28192626 .
AntonioA. Bulbena AntonioA. i inni, Psychiatric and psychological aspects in the Ehlers–Danlos syndromes, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175C (1), 2017, s. 237-245, DOI: 10.1002/ajmg.c.31544, PMID: 28186381 .

ehlers-danlos.com.pl

OlgaO. Haus OlgaO., Nowa Klasyfikacja Zespołu Ehlersa Danlosa [online], Prezentacja przedstawiona podczas I Bydgoskiego Spotkania Osób z Zespołem Ehlersa-Danlosa, 20 maja 2017 [dostęp 2019-08-10] .
Stowarzyszenie chorych na Zespół Ehlersa-Danlosa [online] [dostęp 2019-08-10] .

medicinaneisecoli.it

CristinaC. Brazzaventre CristinaC. i inni, La sindrome di Ehlers-Danlos: storia di un'endiadi clinica da ippocrate a paganini, „Medicina Nei Secoli”, 25 (2), 2013, s. 491–501, PMID: 25807780 [dostęp 2019-08-10] (wł.).

nih.gov

ncbi.nlm.nih.gov

Peter H.P.H. Byers Peter H.P.H. i inni, Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome, „American Journal of Medical Genetics. Part C, Seminars in Medical Genetics”, 175 (1), 2017, s. 40–47, DOI: 10.1002/ajmg.c.31553, PMID: 28306228 .
CristinaC. Brazzaventre CristinaC. i inni, La sindrome di Ehlers-Danlos: storia di un'endiadi clinica da ippocrate a paganini, „Medicina Nei Secoli”, 25 (2), 2013, s. 491–501, PMID: 25807780 [dostęp 2019-08-10] (wł.).
A.P.A.P. Barabas A.P.A.P., Heterogeneity of the Ehlers-Danlos syndrome: description of three clinical types and a hypothesis to explain the basic defect(s), „British Medical Journal”, 2 (5552), 1967, s. 612–613, DOI: 10.1136/bmj.2.5552.612, PMID: 6025600, PMCID: PMC1842124 .
P.P. Beighton P.P. i inni, International Nosology of Heritable Disorders of Connective Tissue, Berlin, 1986, „American Journal of Medical Genetics”, 29 (3), 1988, s. 581–594, DOI: 10.1002/ajmg.1320290316, PMID: 3287925 .
P.P. Beighton P.P. i inni, Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK), „American Journal of Medical Genetics”, 77 (1), 1999, s. 31–37, DOI: 10.1002/(SICI)1096-8628(19980428)77:1<31::AID-AJMG8>3.0.CO;2-O, PMID: 9557891 .
FransiskaF. Malfait FransiskaF. i inni, The 2017 international classification of the Ehlers-Danlos syndromes, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175 (C), 2017, DOI: 10.1002/ajmg.c.31552, PMID: 28306229 .
Patrick R.P.R. Blackburn Patrick R.P.R., Bi-allelic Alterations in AEBP1 Lead to Defective Collagen Assembly and Connective Tissue Structure Resulting in a Variant of Ehlers-Danlos Syndrome, „The American Journal of Human Genetics”, 102 (4), 2018, s. 696-705, DOI: 10.1016/j.ajhg.2018.02.018, PMID: 29606302, PMCID: PMC5985336 .
P.P. Beighton P.P., Hypermobility scoring, „British Journal of Rheumatology”, 27 (2), 1988, s. 163, DOI: 10.1093/rheumatology/27.2.163, PMID: 3365538 .
Dominique P.D.P. Germain Dominique P.D.P., Ehlers-Danlos syndrome type IV, „Orphanet Journal of Rare Diseases”, 2, 2007, s. 32, DOI: 10.1186/1750-1172-2-32, PMID: 17640391, PMCID: PMC1971255 .
Fraser C.F.C. Henderson Fraser C.F.C., Neurological and spinal manifestations of the Ehlers-Danlos syndromes, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175 (1), 2017, s. 195-211, DOI: 10.1002/ajmg.c.31549, PMID: 28220607 .
William B.W.B. Ericson William B.W.B., jr., RogerR. Wolman RogerR., Orthopaedic Management of the Ehlers–Danlos Syndromes, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175 (1), 2017, s. 188–194, DOI: 10.1002/ajmg.c.31551, PMID: 28192621 .
AsmaA. Fikree AsmaA., Gastrointestinal involvement in the Ehlers–Danlos syndromes, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175 (1), 2017, s. 181-187, DOI: 10.1002/ajmg.c.31546, PMID: 28186368 .
AlanA. Hakim AlanA., Cardiovascular autonomic dysfunction in Ehlers–Danlos syndrome—Hypermobile type, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175 (1), 2017, s. 168-174, DOI: 10.1002/ajmg.c.31543, PMID: 28160388 .
AlanA. Hakim AlanA., Chronic fatigue in Ehlers–Danlos syndrome—Hypermobile type, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175 (1), 2017, s. 175-180, DOI: 10.1002/ajmg.c.31542, PMID: 28186393 .
Suranjith L.S.L. Seneviratne Suranjith L.S.L., AnneA. Maitland AnneA., LawrenceL. Afrin LawrenceL., Mast cell disorders in Ehlers–Danlos syndrome, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175C (1), 2017, s. 226-236, DOI: 10.1002/ajmg.c.31555, PMID: 28261938 .
JohnJ. Mitakides JohnJ., Oral and mandibular manifestations in the Ehlers–Danlos syndromes, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175 (1), 2017, s. 220-225, DOI: 10.1002/ajmg.c.31541, PMID: 28192626 .
AntonioA. Bulbena AntonioA. i inni, Psychiatric and psychological aspects in the Ehlers–Danlos syndromes, „American Journal of Medical Genetics Part C (Seminars in Medical Genetics)”, 175C (1), 2017, s. 237-245, DOI: 10.1002/ajmg.c.31544, PMID: 28186381 .

univ-paris5.fr

web2.bium.univ-paris5.fr

E.L.E.L. Ehlers E.L.E.L., Cutis laxa. Neigung zu Haemorrhagien in der Haut, Lockering mehrerer Artikulationen, „Dermatologische Zeitschrift”, 8 (2), 1901, s. 173-174, DOI: 10.1159/000241857 [dostęp 2019-08-10] .
H.H. Danlos H.H., Un cas de cutis laxa avec tumeurs par contusion chronique des coudes et des genoux (xanthome juvénile pseudo-diabetique de MM Hallopeau et Macé de Lépinay), „Bulletin de la Societé francaise de dermatologie et de syphiligraphie”, 19, 1908, s. 70-72 [dostęp 2019-08-10] .