Behr syndrome (English Wikipedia)

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

refsWebsite

Global rank English rank

9doi.org

2^nd place

9nih.gov

4^th place

7worldcat.org

5^th place

3semanticscholar.org

11^th place

8^th place

1whonamedit.com

2,888^th place

2,730^th place

doi.org

Felicio, Andre C.; Godeiro-Junior, Clecio; Alberto, Lucianna G.; Pinto, Aline P. M.; Sallum, Juliana M. F.; Teive, Helio G.; Barsottini, Orlando G. P. (2008-01-01). "Familial Behr syndrome-like phenotype with autosomal dominant inheritance". Parkinsonism & Related Disorders. 14 (4): 370–372. doi:10.1016/j.parkreldis.2007.08.008. ISSN 1353-8020. PMID 17977780.
Marelli, Cecilia; Amati-Bonneau, Patrizia; Reynier, Pascal; Layet, Valérie; Layet, Antoine; Stevanin, Giovanni; Brissaud, Etienne; Bonneau, Dominique; Durr, Alexandra (2011-04-01). "Heterozygous OPA1 mutations in Behr syndrome". Brain. 134 (Pt 4): e169, author reply e170. doi:10.1093/brain/awq306. ISSN 1460-2156. PMID 21112924.
Kleffner, Ilka; Wessling, Caroline; Gess, Burkhard; Korsukewitz, Catharina; Allkemper, Thomas; Schirmacher, Anja; Young, Peter; Senderek, Jan; Husstedt, Ingo W. (2015-10-15). "Behr syndrome with homozygous C19ORF12 mutation". Journal of the Neurological Sciences. 357 (1–2): 115–118. doi:10.1016/j.jns.2015.07.009. ISSN 1878-5883. PMID 26187298. S2CID 30246467.
Schramm, P.; Scheihing, M.; Rasche, D.; Tronnier, V. M. (2005-06-01). "Behr syndrome variant with tremor treated by VIM stimulation". Acta Neurochirurgica. 147 (6): 679–683, discussion 683. doi:10.1007/s00701-005-0508-4. ISSN 0001-6268. PMID 15770348. S2CID 22966348.
Copeliovitch, L.; Katz, K.; Arbel, N.; Harries, N.; Bar-On, E.; Soudry, M. (2001-08-01). "Musculoskeletal deformities in Behr syndrome". Journal of Pediatric Orthopedics. 21 (4): 512–514. doi:10.1097/01241398-200107000-00018. ISSN 0271-6798. PMID 11433166.
Alfaro, José J.; Aparicio, Manuel; Quintana, Alicia; Barrio, Raquel (2002-05-25). "[Behr syndrome and hypergonadotropic hypogonadism]". Medicina Clínica. 118 (19): 759. doi:10.1016/s0025-7753(02)72522-0. ISSN 0025-7753. PMID 12049713.
Bonneau, Dominique; Colin, Estelle; Oca, Florine; Ferré, Marc; Chevrollier, Arnaud; Guéguen, Naïg; Desquiret-Dumas, Valérie; N'Guyen, Sylvie; Barth, Magalie (2014-10-01). "Early-onset Behr syndrome due to compound heterozygous mutations in OPA1". Brain. 137 (Pt 10): e301. doi:10.1093/brain/awu184. ISSN 1460-2156. PMID 25012220.
Horoupian, DS (1979). "Behr syndrome: a clinicopathologic report". Neurology. 29 (3): 323–7. doi:10.1212/wnl.29.3.323. PMID 571977. S2CID 33432542.
Marzan, KA (1994). "MRI abnormalities in Behr syndrome". Pediatr Neurol. 10 (3): 247–8. doi:10.1016/0887-8994(94)90033-7. PMID 8060430.

nih.gov

pubmed.ncbi.nlm.nih.gov

Felicio, Andre C.; Godeiro-Junior, Clecio; Alberto, Lucianna G.; Pinto, Aline P. M.; Sallum, Juliana M. F.; Teive, Helio G.; Barsottini, Orlando G. P. (2008-01-01). "Familial Behr syndrome-like phenotype with autosomal dominant inheritance". Parkinsonism & Related Disorders. 14 (4): 370–372. doi:10.1016/j.parkreldis.2007.08.008. ISSN 1353-8020. PMID 17977780.
Marelli, Cecilia; Amati-Bonneau, Patrizia; Reynier, Pascal; Layet, Valérie; Layet, Antoine; Stevanin, Giovanni; Brissaud, Etienne; Bonneau, Dominique; Durr, Alexandra (2011-04-01). "Heterozygous OPA1 mutations in Behr syndrome". Brain. 134 (Pt 4): e169, author reply e170. doi:10.1093/brain/awq306. ISSN 1460-2156. PMID 21112924.
Kleffner, Ilka; Wessling, Caroline; Gess, Burkhard; Korsukewitz, Catharina; Allkemper, Thomas; Schirmacher, Anja; Young, Peter; Senderek, Jan; Husstedt, Ingo W. (2015-10-15). "Behr syndrome with homozygous C19ORF12 mutation". Journal of the Neurological Sciences. 357 (1–2): 115–118. doi:10.1016/j.jns.2015.07.009. ISSN 1878-5883. PMID 26187298. S2CID 30246467.
Schramm, P.; Scheihing, M.; Rasche, D.; Tronnier, V. M. (2005-06-01). "Behr syndrome variant with tremor treated by VIM stimulation". Acta Neurochirurgica. 147 (6): 679–683, discussion 683. doi:10.1007/s00701-005-0508-4. ISSN 0001-6268. PMID 15770348. S2CID 22966348.
Copeliovitch, L.; Katz, K.; Arbel, N.; Harries, N.; Bar-On, E.; Soudry, M. (2001-08-01). "Musculoskeletal deformities in Behr syndrome". Journal of Pediatric Orthopedics. 21 (4): 512–514. doi:10.1097/01241398-200107000-00018. ISSN 0271-6798. PMID 11433166.
Alfaro, José J.; Aparicio, Manuel; Quintana, Alicia; Barrio, Raquel (2002-05-25). "[Behr syndrome and hypergonadotropic hypogonadism]". Medicina Clínica. 118 (19): 759. doi:10.1016/s0025-7753(02)72522-0. ISSN 0025-7753. PMID 12049713.
Bonneau, Dominique; Colin, Estelle; Oca, Florine; Ferré, Marc; Chevrollier, Arnaud; Guéguen, Naïg; Desquiret-Dumas, Valérie; N'Guyen, Sylvie; Barth, Magalie (2014-10-01). "Early-onset Behr syndrome due to compound heterozygous mutations in OPA1". Brain. 137 (Pt 10): e301. doi:10.1093/brain/awu184. ISSN 1460-2156. PMID 25012220.
Horoupian, DS (1979). "Behr syndrome: a clinicopathologic report". Neurology. 29 (3): 323–7. doi:10.1212/wnl.29.3.323. PMID 571977. S2CID 33432542.
Marzan, KA (1994). "MRI abnormalities in Behr syndrome". Pediatr Neurol. 10 (3): 247–8. doi:10.1016/0887-8994(94)90033-7. PMID 8060430.

semanticscholar.org

api.semanticscholar.org

Kleffner, Ilka; Wessling, Caroline; Gess, Burkhard; Korsukewitz, Catharina; Allkemper, Thomas; Schirmacher, Anja; Young, Peter; Senderek, Jan; Husstedt, Ingo W. (2015-10-15). "Behr syndrome with homozygous C19ORF12 mutation". Journal of the Neurological Sciences. 357 (1–2): 115–118. doi:10.1016/j.jns.2015.07.009. ISSN 1878-5883. PMID 26187298. S2CID 30246467.
Schramm, P.; Scheihing, M.; Rasche, D.; Tronnier, V. M. (2005-06-01). "Behr syndrome variant with tremor treated by VIM stimulation". Acta Neurochirurgica. 147 (6): 679–683, discussion 683. doi:10.1007/s00701-005-0508-4. ISSN 0001-6268. PMID 15770348. S2CID 22966348.
Horoupian, DS (1979). "Behr syndrome: a clinicopathologic report". Neurology. 29 (3): 323–7. doi:10.1212/wnl.29.3.323. PMID 571977. S2CID 33432542.

whonamedit.com

synd/3048 at Who Named It?

worldcat.org

search.worldcat.org

Felicio, Andre C.; Godeiro-Junior, Clecio; Alberto, Lucianna G.; Pinto, Aline P. M.; Sallum, Juliana M. F.; Teive, Helio G.; Barsottini, Orlando G. P. (2008-01-01). "Familial Behr syndrome-like phenotype with autosomal dominant inheritance". Parkinsonism & Related Disorders. 14 (4): 370–372. doi:10.1016/j.parkreldis.2007.08.008. ISSN 1353-8020. PMID 17977780.
Marelli, Cecilia; Amati-Bonneau, Patrizia; Reynier, Pascal; Layet, Valérie; Layet, Antoine; Stevanin, Giovanni; Brissaud, Etienne; Bonneau, Dominique; Durr, Alexandra (2011-04-01). "Heterozygous OPA1 mutations in Behr syndrome". Brain. 134 (Pt 4): e169, author reply e170. doi:10.1093/brain/awq306. ISSN 1460-2156. PMID 21112924.
Kleffner, Ilka; Wessling, Caroline; Gess, Burkhard; Korsukewitz, Catharina; Allkemper, Thomas; Schirmacher, Anja; Young, Peter; Senderek, Jan; Husstedt, Ingo W. (2015-10-15). "Behr syndrome with homozygous C19ORF12 mutation". Journal of the Neurological Sciences. 357 (1–2): 115–118. doi:10.1016/j.jns.2015.07.009. ISSN 1878-5883. PMID 26187298. S2CID 30246467.
Schramm, P.; Scheihing, M.; Rasche, D.; Tronnier, V. M. (2005-06-01). "Behr syndrome variant with tremor treated by VIM stimulation". Acta Neurochirurgica. 147 (6): 679–683, discussion 683. doi:10.1007/s00701-005-0508-4. ISSN 0001-6268. PMID 15770348. S2CID 22966348.
Copeliovitch, L.; Katz, K.; Arbel, N.; Harries, N.; Bar-On, E.; Soudry, M. (2001-08-01). "Musculoskeletal deformities in Behr syndrome". Journal of Pediatric Orthopedics. 21 (4): 512–514. doi:10.1097/01241398-200107000-00018. ISSN 0271-6798. PMID 11433166.
Alfaro, José J.; Aparicio, Manuel; Quintana, Alicia; Barrio, Raquel (2002-05-25). "[Behr syndrome and hypergonadotropic hypogonadism]". Medicina Clínica. 118 (19): 759. doi:10.1016/s0025-7753(02)72522-0. ISSN 0025-7753. PMID 12049713.
Bonneau, Dominique; Colin, Estelle; Oca, Florine; Ferré, Marc; Chevrollier, Arnaud; Guéguen, Naïg; Desquiret-Dumas, Valérie; N'Guyen, Sylvie; Barth, Magalie (2014-10-01). "Early-onset Behr syndrome due to compound heterozygous mutations in OPA1". Brain. 137 (Pt 10): e301. doi:10.1093/brain/awu184. ISSN 1460-2156. PMID 25012220.