Central hypoventilation syndrome (English Wikipedia)

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

refsWebsite

Global rank English rank

18nih.gov

4^th place

15doi.org

2^nd place

3semanticscholar.org

11^th place

8^th place

2medscape.com

719^th place

636^th place

1cchsnetwork.org

low place

1accessmedicine.com

low place

1bbc.co.uk

8^th place

10^th place

1worldcat.org

5^th place

1go.com

48^th place

39^th place

accessmedicine.com

Longo, Dan L. (2012). "Chapter 264. Disorders of Ventilation". Harrison's principles of internal medicine (18th ed.). New York: McGraw-Hill. ISBN 9780071748896.

bbc.co.uk

news.bbc.co.uk

"Gene secret of 'mythical curse'". BBC News. 5 May 2003. (The article misspells PHOX2B as "Thox2b".)

cchsnetwork.org

"CCHS Network | Casting a Light in the Dark". CCHS Network.

doi.org

Windisch W, Hennings E, Storre J, Matthys H, Sorichter S (2004). "Long-term survival of a patient with congenital central hypoventilation syndrome despite the lack of continuous ventilatory support". Respiration. 71 (2): 195–8. doi:10.1159/000076685. PMID 15031579. S2CID 36554567.
Bygarski, Elizabeth; Paterson, Melanie; Lemire, Edmond G. (April 26, 2013). "Extreme intra-familial variability of congenital central hypoventilation syndrome: a case series". Journal of Medical Case Reports. 7 (1): 117. doi:10.1186/1752-1947-7-117. PMC 3651317. PMID 23622117.
Lovell BL, Bullock RE, Anderson KN (March 2010). "An unusual presentation of congenital central hypoventilation syndrome (Ondine's Curse)". Emerg Med J. 27 (3): 237–8. doi:10.1136/emj.2009.072215. PMID 20304901. S2CID 206938512.
Trang H, Dehan M, Beaufils F, Zaccaria I, Amiel J, Gaultier C (2005). "The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype". Chest. 127 (1): 72–9. doi:10.1378/chest.127.1.72. PMID 15653965.
Long, K. J.; Allen, N. (October 1984). "Abnormal brain-stem auditory evoked potentials following Ondine's curse". Arch. Neurol. 41 (10): 1109–10. doi:10.1001/archneur.1984.04050210111028. PMID 6477223.
Gaultier C; Amiel J; Dauger S; et al. (2004). "Genetics and early disturbances of breathing control". Pediatr. Res. 55 (5): 729–33. doi:10.1203/01.PDR.0000115677.78759.C5. PMID 14739359.
Gaultier C, Trang H, Dauger S, Gallego J (2005). "Pediatric disorders with autonomic dysfunction: what role for PHOX2B?". Pediatr. Res. 58 (1): 1–6. doi:10.1203/01.PDR.0000166755.29277.C4. PMID 15901893.
Todd ES, Weinberg SM, Berry-Kravis EM, et al. (2006). "Facial phenotype in children and young adults with PHOX2B-determined congenital central hypoventilation syndrome: quantitative pattern of dysmorphology". Pediatr. Res. 59 (1): 39–45. doi:10.1203/01.pdr.0000191814.73340.1d. PMID 16327002.
Lake, Jonathan; Heuckeroth, Robert (July 2013). "Enteric nervous system development: migration, differentiation, and disease". American Journal of Physiology. Gastrointestinal and Liver Physiology. 305 (1): G1–G24. doi:10.1152/ajpgi.00452.2012. PMC 3725693. PMID 23639815.
Kincaid PK, Dietrich RB, Pais MJ (1994). "Pediatric case of the day. Neurocristopathy (Ondine-Hirschsprung syndrome)". Radiographics. 14 (5): 1139–43. doi:10.1148/radiographics.14.5.7991820. PMID 7991820.
Poceta, J. S.; Strandjord, T. P.; Badura, R. J.; Milstein, J. M. (1987). "Undine curse and neurocristopathy". Pediatr. Neurol. 3 (6): 370–2. doi:10.1016/0887-8994(87)90011-7. PMID 3508086.
Zaidi, Saher; Gandhi, Jason; Vatsia, Sohrab; Smith, Noel L.; Khan, Sardar Ali (March 2018). "Congenital central hypoventilation syndrome: An overview of etiopathogenesis, associated pathologies, clinical presentation, and management". Autonomic Neuroscience. 210: 1–9. doi:10.1016/j.autneu.2017.11.003. ISSN 1566-0702. PMID 29249648. S2CID 4435638.
Takeda, S.; Fujii, Y.; Kawahara, H.; Nakahara, K.; Matsuda H. (1996). "Central alveolar hypoventilation syndrome (Undine's curse) with gastroesophageal reflux". Chest. 110 (3): 850–852. doi:10.1378/chest.110.3.850. PMID 8797441.
Sugar, Oscar (1978). "In Search of Ondine's Curse". JAMA. 1978, 240 (3): 236–237. doi:10.1001/jama.1978.03290030054019. PMID 351225.

dx.doi.org

Zaidi, Saher; Gandhi, Jason; Vatsia, Sohrab; Smith, Noel L.; Khan, Sardar Ali (March 2018). "Congenital central hypoventilation syndrome: An overview of etiopathogenesis, associated pathologies, clinical presentation, and management". Autonomic Neuroscience. 210: 1–9. doi:10.1016/j.autneu.2017.11.003. ISSN 1566-0702. PMID 29249648. S2CID 4435638.

go.com

abcnews.go.com

"Death by Nap: Boy Risks Death if He Nods off". ABC News. 2010-08-17.

medscape.com

emedicine.medscape.com

Jazeela Fayyaz, DO (2017-12-05). Zab Mosenifar, M (ed.). "Hypoventilation Syndromes". Medscape.
Congenital Central Hypoventilation Syndrome at eMedicine

nih.gov

pubmed.ncbi.nlm.nih.gov

Windisch W, Hennings E, Storre J, Matthys H, Sorichter S (2004). "Long-term survival of a patient with congenital central hypoventilation syndrome despite the lack of continuous ventilatory support". Respiration. 71 (2): 195–8. doi:10.1159/000076685. PMID 15031579. S2CID 36554567.
Bygarski, Elizabeth; Paterson, Melanie; Lemire, Edmond G. (April 26, 2013). "Extreme intra-familial variability of congenital central hypoventilation syndrome: a case series". Journal of Medical Case Reports. 7 (1): 117. doi:10.1186/1752-1947-7-117. PMC 3651317. PMID 23622117.
Lovell BL, Bullock RE, Anderson KN (March 2010). "An unusual presentation of congenital central hypoventilation syndrome (Ondine's Curse)". Emerg Med J. 27 (3): 237–8. doi:10.1136/emj.2009.072215. PMID 20304901. S2CID 206938512.
Trang H, Dehan M, Beaufils F, Zaccaria I, Amiel J, Gaultier C (2005). "The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype". Chest. 127 (1): 72–9. doi:10.1378/chest.127.1.72. PMID 15653965.
Long, K. J.; Allen, N. (October 1984). "Abnormal brain-stem auditory evoked potentials following Ondine's curse". Arch. Neurol. 41 (10): 1109–10. doi:10.1001/archneur.1984.04050210111028. PMID 6477223.
Gaultier C; Amiel J; Dauger S; et al. (2004). "Genetics and early disturbances of breathing control". Pediatr. Res. 55 (5): 729–33. doi:10.1203/01.PDR.0000115677.78759.C5. PMID 14739359.
Gaultier C, Trang H, Dauger S, Gallego J (2005). "Pediatric disorders with autonomic dysfunction: what role for PHOX2B?". Pediatr. Res. 58 (1): 1–6. doi:10.1203/01.PDR.0000166755.29277.C4. PMID 15901893.
Todd ES, Weinberg SM, Berry-Kravis EM, et al. (2006). "Facial phenotype in children and young adults with PHOX2B-determined congenital central hypoventilation syndrome: quantitative pattern of dysmorphology". Pediatr. Res. 59 (1): 39–45. doi:10.1203/01.pdr.0000191814.73340.1d. PMID 16327002.
Lake, Jonathan; Heuckeroth, Robert (July 2013). "Enteric nervous system development: migration, differentiation, and disease". American Journal of Physiology. Gastrointestinal and Liver Physiology. 305 (1): G1–G24. doi:10.1152/ajpgi.00452.2012. PMC 3725693. PMID 23639815.
Kincaid PK, Dietrich RB, Pais MJ (1994). "Pediatric case of the day. Neurocristopathy (Ondine-Hirschsprung syndrome)". Radiographics. 14 (5): 1139–43. doi:10.1148/radiographics.14.5.7991820. PMID 7991820.
Poceta, J. S.; Strandjord, T. P.; Badura, R. J.; Milstein, J. M. (1987). "Undine curse and neurocristopathy". Pediatr. Neurol. 3 (6): 370–2. doi:10.1016/0887-8994(87)90011-7. PMID 3508086.
Zaidi, Saher; Gandhi, Jason; Vatsia, Sohrab; Smith, Noel L.; Khan, Sardar Ali (March 2018). "Congenital central hypoventilation syndrome: An overview of etiopathogenesis, associated pathologies, clinical presentation, and management". Autonomic Neuroscience. 210: 1–9. doi:10.1016/j.autneu.2017.11.003. ISSN 1566-0702. PMID 29249648. S2CID 4435638.
Takeda, S.; Fujii, Y.; Kawahara, H.; Nakahara, K.; Matsuda H. (1996). "Central alveolar hypoventilation syndrome (Undine's curse) with gastroesophageal reflux". Chest. 110 (3): 850–852. doi:10.1378/chest.110.3.850. PMID 8797441.
Sugar, Oscar (1978). "In Search of Ondine's Curse". JAMA. 1978, 240 (3): 236–237. doi:10.1001/jama.1978.03290030054019. PMID 351225.

ncbi.nlm.nih.gov

Bygarski, Elizabeth; Paterson, Melanie; Lemire, Edmond G. (April 26, 2013). "Extreme intra-familial variability of congenital central hypoventilation syndrome: a case series". Journal of Medical Case Reports. 7 (1): 117. doi:10.1186/1752-1947-7-117. PMC 3651317. PMID 23622117.
"Primary alveolar hypoventilation: Ondine's curse". A.D.A.M. Medical Encyclopedia. U.S. National Library of Medicine. September 17, 2010.
Lake, Jonathan; Heuckeroth, Robert (July 2013). "Enteric nervous system development: migration, differentiation, and disease". American Journal of Physiology. Gastrointestinal and Liver Physiology. 305 (1): G1–G24. doi:10.1152/ajpgi.00452.2012. PMC 3725693. PMID 23639815.

ghr.nlm.nih.gov

"Congenital central hypoventilation syndrome". Genetics Home Reference. U.S. National Library of Medicine. Retrieved 5 June 2015.

semanticscholar.org

api.semanticscholar.org

Windisch W, Hennings E, Storre J, Matthys H, Sorichter S (2004). "Long-term survival of a patient with congenital central hypoventilation syndrome despite the lack of continuous ventilatory support". Respiration. 71 (2): 195–8. doi:10.1159/000076685. PMID 15031579. S2CID 36554567.
Lovell BL, Bullock RE, Anderson KN (March 2010). "An unusual presentation of congenital central hypoventilation syndrome (Ondine's Curse)". Emerg Med J. 27 (3): 237–8. doi:10.1136/emj.2009.072215. PMID 20304901. S2CID 206938512.
Zaidi, Saher; Gandhi, Jason; Vatsia, Sohrab; Smith, Noel L.; Khan, Sardar Ali (March 2018). "Congenital central hypoventilation syndrome: An overview of etiopathogenesis, associated pathologies, clinical presentation, and management". Autonomic Neuroscience. 210: 1–9. doi:10.1016/j.autneu.2017.11.003. ISSN 1566-0702. PMID 29249648. S2CID 4435638.

worldcat.org

search.worldcat.org

Zaidi, Saher; Gandhi, Jason; Vatsia, Sohrab; Smith, Noel L.; Khan, Sardar Ali (March 2018). "Congenital central hypoventilation syndrome: An overview of etiopathogenesis, associated pathologies, clinical presentation, and management". Autonomic Neuroscience. 210: 1–9. doi:10.1016/j.autneu.2017.11.003. ISSN 1566-0702. PMID 29249648. S2CID 4435638.