Sindrom Ehlers-Danlos (Indonesian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sindrom Ehlers-Danlos" in Indonesian language version.

refsWebsite

Global rank Indonesian rank

9nih.gov

4^th place

13^th place

6doi.org

2^nd place

4^th place

6worldcat.org

5^th place

7^th place

2ehlers-danlos.com

low place

2medlineplus.gov

1,581^st place

2,421^st place

2wiley.com

222^nd place

280^th place

2ehlersdanlosnews.com

low place

1thevedsmovement.org

low place

1alodokter.com

low place

676^th place

1orpha.net

3,537^th place

low place

1bmj.com

1,226^th place

1,806^th place

alodokter.com

Willy, Tjin (27 Januari 2017). "Pectus Excavatum". Alodokter. Diakses tanggal 2 Maret 2022.

bmj.com

jmg.bmj.com

Minatogawa, Mari; Unzaki, Ai; Morisaki, Hiroko; Syx, Delfien; Sonoda, Tohru; Janecke, Andreas R.; Slavotinek, Anne; Voermans, Nicol C.; Lacassie, Yves (22 November 2021). "Clinical and molecular features of 66 patients with musculocontractural Ehlers−Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14)". Journal of Medical Genetics. doi:10.1136/jmedgenet-2020-107623. ISSN 0022-2593.

doi.org

Bowen, Jessica M.; Sobey, Glenda J.; Burrows, Nigel P.; Colombi, Marina; Lavallee, Mark E.; Malfait, Fransiska; Francomano, Clair A. (13 Februari 2017). "Ehlers-Danlos syndrome, classical type". American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 175 (1): 27–39. doi:10.1002/ajmg.c.31548. ISSN 1552-4868.
Ritelli, Marco; Venturini, Marina; Cinquina, Valeria; Chiarelli, Nicola; Colombi, Marina (31 Juli 2020). "Multisystemic manifestations in a cohort of 75 classical Ehlers-Danlos syndrome patients: natural history and nosological perspectives". Orphanet Journal of Rare Diseases. 15 (1): 197. doi:10.1186/s13023-020-01470-0. ISSN 1750-1172. PMC 7393722 . PMID 32736638. Pemeliharaan CS1: Format PMC (link)
Malfait, Fransiska; Francomano, Clair; Byers, Peter; Belmont, John; Berglund, Britta; Black, James; Bloom, Lara; Bowen, Jessica M.; Brady, Angela F. (2017-03). "The 2017 international classification of the Ehlers-Danlos syndromes". American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 175 (1): 8–26. doi:10.1002/ajmg.c.31552. ISSN 1552-4868.
Burkitt Wright, Emma MM; Porter, Louise F.; Spencer, Helen L.; Clayton-Smith, Jill; Au, Leon; Munier, Francis L.; Smithson, Sarah; Suri, Mohnish; Rohrbach, Marianne (2013-05-04). "Brittle cornea syndrome: recognition, molecular diagnosis and management". Orphanet Journal of Rare Diseases. 8 (1): 68. doi:10.1186/1750-1172-8-68. ISSN 1750-1172. PMC 3659006 . PMID 23642083. Pemeliharaan CS1: Format PMC (link)
Lorenz, Delia; Kress, Wolfram; Zaum, Ann-Kathrin; Speer, Christian P.; Hebestreit, Helge (2021-06-30). "Report of two siblings with spondylodysplastic Ehlers-Danlos syndrome and B4GALT7 deficiency". BMC Pediatrics. 21 (1): 293. doi:10.1186/s12887-021-02767-0. ISSN 1471-2431.
Minatogawa, Mari; Unzaki, Ai; Morisaki, Hiroko; Syx, Delfien; Sonoda, Tohru; Janecke, Andreas R.; Slavotinek, Anne; Voermans, Nicol C.; Lacassie, Yves (22 November 2021). "Clinical and molecular features of 66 patients with musculocontractural Ehlers−Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14)". Journal of Medical Genetics. doi:10.1136/jmedgenet-2020-107623. ISSN 0022-2593.

ehlers-danlos.com

"What are the Ehlers-Danlos Syndromes?". The Ehlers Danlos Society. Diakses tanggal 28 Februari 2022.
"The Types of EDS". The Ehlers Danlos Society. Diakses tanggal 28 Februari 2022.

ehlersdanlosnews.com

Malcolm, Emily. "Dermatosparaxis EDS – Ehlers-Danlos News". ehlersdanlosnews. Diakses tanggal 28 Februari 2022.
DSouza, Anthony Deepak. "Myopathic EDS – Ehlers-Danlos News". Diakses tanggal 28 Oktober 2022.

medlineplus.gov

"Ehlers-Danlos syndrome: MedlinePlus Genetics". medlineplus.gov. Diakses tanggal 2 Maret 2022.
"Craniofacial Abnormalities". medlineplus.gov. Diakses tanggal 28 Februari 2022.

nih.gov

rarediseases.info.nih.gov

"Classical-like Ehlers-Danlos syndrome". www.raredisease.info.nih.gov. Diakses tanggal 28 Februari 2022.
"Cardiac-Valvular Ehlers-Danlos syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Diakses tanggal 28 Februari 2022.
"Vascular Ehlers-Danlos syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Diakses tanggal 28 Februari 2022.
"Hypermobile Ehlers-Danlos syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Diakses tanggal 28 Februari 2022.
"Kyphoscoliotic Ehlers-Danlos syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Diakses tanggal 28 Februari 2022.

ncbi.nlm.nih.gov

Malfait, Fransiska; Wenstrup, Richard; De Paepe, Anne (1993). Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E.; Bean, Lora JH; Gripp, Karen W.; Mirzaa, Ghayda M.; Amemiya, Anne, ed. Classic Ehlers-Danlos Syndrome. Seattle (WA): University of Washington, Seattle. PMID 20301422.
Ritelli, Marco; Venturini, Marina; Cinquina, Valeria; Chiarelli, Nicola; Colombi, Marina (31 Juli 2020). "Multisystemic manifestations in a cohort of 75 classical Ehlers-Danlos syndrome patients: natural history and nosological perspectives". Orphanet Journal of Rare Diseases. 15 (1): 197. doi:10.1186/s13023-020-01470-0. ISSN 1750-1172. PMC 7393722 . PMID 32736638. Pemeliharaan CS1: Format PMC (link)
Burkitt Wright, Emma MM; Porter, Louise F.; Spencer, Helen L.; Clayton-Smith, Jill; Au, Leon; Munier, Francis L.; Smithson, Sarah; Suri, Mohnish; Rohrbach, Marianne (2013-05-04). "Brittle cornea syndrome: recognition, molecular diagnosis and management". Orphanet Journal of Rare Diseases. 8 (1): 68. doi:10.1186/1750-1172-8-68. ISSN 1750-1172. PMC 3659006 . PMID 23642083. Pemeliharaan CS1: Format PMC (link)
Kapferer-Seebacher, Ines; van Dijk, Fleur S.; Zschocke, Johannes (1993). Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E.; Bean, Lora JH; Gripp, Karen W.; Mirzaa, Ghayda M.; Amemiya, Anne, ed. Periodontal Ehlers-Danlos Syndrome. Seattle (WA): University of Washington, Seattle.

orpha.net

"Orphanet: Arthrochalasia Ehlers Danlos syndrome". www.orpha.net. Diakses tanggal 2022-02-28.

thevedsmovement.org

"Symptoms of Vascular Ehlers-Danlos syndrome". The VEDS Movement (dalam bahasa Inggris). Diakses tanggal 2022-02-28.

wiley.com

onlinelibrary.wiley.com

Bowen, Jessica M.; Sobey, Glenda J.; Burrows, Nigel P.; Colombi, Marina; Lavallee, Mark E.; Malfait, Fransiska; Francomano, Clair A. (13 Februari 2017). "Ehlers-Danlos syndrome, classical type". American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 175 (1): 27–39. doi:10.1002/ajmg.c.31548. ISSN 1552-4868.
Malfait, Fransiska; Francomano, Clair; Byers, Peter; Belmont, John; Berglund, Britta; Black, James; Bloom, Lara; Bowen, Jessica M.; Brady, Angela F. (2017-03). "The 2017 international classification of the Ehlers-Danlos syndromes". American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 175 (1): 8–26. doi:10.1002/ajmg.c.31552. ISSN 1552-4868.

worldcat.org

Bowen, Jessica M.; Sobey, Glenda J.; Burrows, Nigel P.; Colombi, Marina; Lavallee, Mark E.; Malfait, Fransiska; Francomano, Clair A. (13 Februari 2017). "Ehlers-Danlos syndrome, classical type". American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 175 (1): 27–39. doi:10.1002/ajmg.c.31548. ISSN 1552-4868.
Ritelli, Marco; Venturini, Marina; Cinquina, Valeria; Chiarelli, Nicola; Colombi, Marina (31 Juli 2020). "Multisystemic manifestations in a cohort of 75 classical Ehlers-Danlos syndrome patients: natural history and nosological perspectives". Orphanet Journal of Rare Diseases. 15 (1): 197. doi:10.1186/s13023-020-01470-0. ISSN 1750-1172. PMC 7393722 . PMID 32736638. Pemeliharaan CS1: Format PMC (link)
Malfait, Fransiska; Francomano, Clair; Byers, Peter; Belmont, John; Berglund, Britta; Black, James; Bloom, Lara; Bowen, Jessica M.; Brady, Angela F. (2017-03). "The 2017 international classification of the Ehlers-Danlos syndromes". American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 175 (1): 8–26. doi:10.1002/ajmg.c.31552. ISSN 1552-4868.
Burkitt Wright, Emma MM; Porter, Louise F.; Spencer, Helen L.; Clayton-Smith, Jill; Au, Leon; Munier, Francis L.; Smithson, Sarah; Suri, Mohnish; Rohrbach, Marianne (2013-05-04). "Brittle cornea syndrome: recognition, molecular diagnosis and management". Orphanet Journal of Rare Diseases. 8 (1): 68. doi:10.1186/1750-1172-8-68. ISSN 1750-1172. PMC 3659006 . PMID 23642083. Pemeliharaan CS1: Format PMC (link)
Lorenz, Delia; Kress, Wolfram; Zaum, Ann-Kathrin; Speer, Christian P.; Hebestreit, Helge (2021-06-30). "Report of two siblings with spondylodysplastic Ehlers-Danlos syndrome and B4GALT7 deficiency". BMC Pediatrics. 21 (1): 293. doi:10.1186/s12887-021-02767-0. ISSN 1471-2431.
Minatogawa, Mari; Unzaki, Ai; Morisaki, Hiroko; Syx, Delfien; Sonoda, Tohru; Janecke, Andreas R.; Slavotinek, Anne; Voermans, Nicol C.; Lacassie, Yves (22 November 2021). "Clinical and molecular features of 66 patients with musculocontractural Ehlers−Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14)". Journal of Medical Genetics. doi:10.1136/jmedgenet-2020-107623. ISSN 0022-2593.