CANDLE syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "CANDLE syndrome" in English language version.

refsWebsite

Global rank English rank

10nih.gov

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7doi.org

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2semanticscholar.org

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doi.org

Tüfekçi Ö, Bengoa Ş, Karapinar TH, Ataseven EB, İrken G, Ören H (May 2015). "CANDLE syndrome: a recently described autoinflammatory syndrome". Journal of Pediatric Hematology/Oncology. 37 (4). Lippincott Williams & Wilkins: 296–299. doi:10.1097/MPH.0000000000000212. PMID 25036278. S2CID 37875499.
Torrelo A, Patel S, Colmenero I, Gurbindo D, Lendínez F, Hernández A, López-Robledillo JC, Dadban A, Requena L, Paller AS (March 2010). "Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome". Journal of the American Academy of Dermatology. 62 (3). Elsevier: 489–495. doi:10.1016/j.jaad.2009.04.046. PMID 20159315.
Roberts T, Stephen L, Scott C, di Pasquale T, Naser-eldin A, Chetty M, Shaik S, Lewandowski L, Beighton P (December 28, 2015). "CANDLE SYNDROME: Orodfacial manifestations and dental implications". Head & Face Medicine. 11 (38). BioMed Central: 38. doi:10.1186/s13005-015-0095-4. PMC 4693439. PMID 26711936.
Cavalcante MP, Brunelli JB, Miranda CC, Novak GV, Malle L, Aikawa NE, Jesus AA, Silva CA (May 2016). "CANDLE syndrome: chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature-a rare case with a novel mutation". European Journal of Pediatrics. 175 (5). Springer Science+Business Media: 735–740. doi:10.1007/s00431-015-2668-4. PMID 26567544. S2CID 20175274.
Brehm A, Liu Y, Sheikh A, Marrero B, Omoyinmi E, Zhou Q, Montealegre G, Biancotto A, Reinhardt A, Almeida de Jesus A, Pelletier M, Tsai WL, Remmers EF, Kardava L, Hill S, Kim H, Lachmann HJ, Megarbane A, Chae JJ, Brady J, Castillo RD, Brown D, Casano AV, Gao L, Chapelle D, Huang Y, Stone D, Chen Y, Sotzny F, Lee CC, Kastner DL, Torrelo A, Zlotogorski A, Moir S, Gadina M, McCoy P, Wesley R, Rother KI, Hildebrand PW, Brogan P, Krüger E, Aksentijevich I, Goldbach-Mansky R (November 2, 2015). "Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production". Journal of Clinical Investigation. 125 (11). American Society for Clinical Investigation: 4196–4211. doi:10.1172/JCI81260. PMC 4639987. PMID 26524591.
Garg A, Hernandez MD, Sousa AB, Subramanyam L, Martínez de Villarreal L, dos Santos HG, Barboza O (September 2010). "An autosomal recessive syndrome of joint contractures, muscular atrophy, microcytic anemia, and panniculitis-associated lipodystrophy". The Journal of Clinical Endocrinology and Metabolism. 95 (9). Endocrine Society: E58-63. doi:10.1210/jc.2010-0488. PMC 2936059. PMID 20534754.
Wang H, Das L, Tan Hung Tiong J, Vasanwala RF, Arkachaisri T (November 2014). "CANDLE syndrome: an extended clinical spectrum". Rheumatology. 53 (11). Oxford University Press: 2119–2120. doi:10.1093/rheumatology/keu298. PMID 25065002.

nih.gov

pubmed.ncbi.nlm.nih.gov

Tüfekçi Ö, Bengoa Ş, Karapinar TH, Ataseven EB, İrken G, Ören H (May 2015). "CANDLE syndrome: a recently described autoinflammatory syndrome". Journal of Pediatric Hematology/Oncology. 37 (4). Lippincott Williams & Wilkins: 296–299. doi:10.1097/MPH.0000000000000212. PMID 25036278. S2CID 37875499.
Torrelo A, Patel S, Colmenero I, Gurbindo D, Lendínez F, Hernández A, López-Robledillo JC, Dadban A, Requena L, Paller AS (March 2010). "Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome". Journal of the American Academy of Dermatology. 62 (3). Elsevier: 489–495. doi:10.1016/j.jaad.2009.04.046. PMID 20159315.
Roberts T, Stephen L, Scott C, di Pasquale T, Naser-eldin A, Chetty M, Shaik S, Lewandowski L, Beighton P (December 28, 2015). "CANDLE SYNDROME: Orodfacial manifestations and dental implications". Head & Face Medicine. 11 (38). BioMed Central: 38. doi:10.1186/s13005-015-0095-4. PMC 4693439. PMID 26711936.
Cavalcante MP, Brunelli JB, Miranda CC, Novak GV, Malle L, Aikawa NE, Jesus AA, Silva CA (May 2016). "CANDLE syndrome: chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature-a rare case with a novel mutation". European Journal of Pediatrics. 175 (5). Springer Science+Business Media: 735–740. doi:10.1007/s00431-015-2668-4. PMID 26567544. S2CID 20175274.
Brehm A, Liu Y, Sheikh A, Marrero B, Omoyinmi E, Zhou Q, Montealegre G, Biancotto A, Reinhardt A, Almeida de Jesus A, Pelletier M, Tsai WL, Remmers EF, Kardava L, Hill S, Kim H, Lachmann HJ, Megarbane A, Chae JJ, Brady J, Castillo RD, Brown D, Casano AV, Gao L, Chapelle D, Huang Y, Stone D, Chen Y, Sotzny F, Lee CC, Kastner DL, Torrelo A, Zlotogorski A, Moir S, Gadina M, McCoy P, Wesley R, Rother KI, Hildebrand PW, Brogan P, Krüger E, Aksentijevich I, Goldbach-Mansky R (November 2, 2015). "Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production". Journal of Clinical Investigation. 125 (11). American Society for Clinical Investigation: 4196–4211. doi:10.1172/JCI81260. PMC 4639987. PMID 26524591.
Garg A, Hernandez MD, Sousa AB, Subramanyam L, Martínez de Villarreal L, dos Santos HG, Barboza O (September 2010). "An autosomal recessive syndrome of joint contractures, muscular atrophy, microcytic anemia, and panniculitis-associated lipodystrophy". The Journal of Clinical Endocrinology and Metabolism. 95 (9). Endocrine Society: E58-63. doi:10.1210/jc.2010-0488. PMC 2936059. PMID 20534754.
Wang H, Das L, Tan Hung Tiong J, Vasanwala RF, Arkachaisri T (November 2014). "CANDLE syndrome: an extended clinical spectrum". Rheumatology. 53 (11). Oxford University Press: 2119–2120. doi:10.1093/rheumatology/keu298. PMID 25065002.

ncbi.nlm.nih.gov

Roberts T, Stephen L, Scott C, di Pasquale T, Naser-eldin A, Chetty M, Shaik S, Lewandowski L, Beighton P (December 28, 2015). "CANDLE SYNDROME: Orodfacial manifestations and dental implications". Head & Face Medicine. 11 (38). BioMed Central: 38. doi:10.1186/s13005-015-0095-4. PMC 4693439. PMID 26711936.
Brehm A, Liu Y, Sheikh A, Marrero B, Omoyinmi E, Zhou Q, Montealegre G, Biancotto A, Reinhardt A, Almeida de Jesus A, Pelletier M, Tsai WL, Remmers EF, Kardava L, Hill S, Kim H, Lachmann HJ, Megarbane A, Chae JJ, Brady J, Castillo RD, Brown D, Casano AV, Gao L, Chapelle D, Huang Y, Stone D, Chen Y, Sotzny F, Lee CC, Kastner DL, Torrelo A, Zlotogorski A, Moir S, Gadina M, McCoy P, Wesley R, Rother KI, Hildebrand PW, Brogan P, Krüger E, Aksentijevich I, Goldbach-Mansky R (November 2, 2015). "Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production". Journal of Clinical Investigation. 125 (11). American Society for Clinical Investigation: 4196–4211. doi:10.1172/JCI81260. PMC 4639987. PMID 26524591.
Garg A, Hernandez MD, Sousa AB, Subramanyam L, Martínez de Villarreal L, dos Santos HG, Barboza O (September 2010). "An autosomal recessive syndrome of joint contractures, muscular atrophy, microcytic anemia, and panniculitis-associated lipodystrophy". The Journal of Clinical Endocrinology and Metabolism. 95 (9). Endocrine Society: E58-63. doi:10.1210/jc.2010-0488. PMC 2936059. PMID 20534754.

semanticscholar.org

api.semanticscholar.org

Tüfekçi Ö, Bengoa Ş, Karapinar TH, Ataseven EB, İrken G, Ören H (May 2015). "CANDLE syndrome: a recently described autoinflammatory syndrome". Journal of Pediatric Hematology/Oncology. 37 (4). Lippincott Williams & Wilkins: 296–299. doi:10.1097/MPH.0000000000000212. PMID 25036278. S2CID 37875499.
Cavalcante MP, Brunelli JB, Miranda CC, Novak GV, Malle L, Aikawa NE, Jesus AA, Silva CA (May 2016). "CANDLE syndrome: chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature-a rare case with a novel mutation". European Journal of Pediatrics. 175 (5). Springer Science+Business Media: 735–740. doi:10.1007/s00431-015-2668-4. PMID 26567544. S2CID 20175274.