Congenital fiber type disproportion (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Congenital fiber type disproportion" in English language version.

refsWebsite

Global rank English rank

7doi.org

2^nd place

7nih.gov

4^th place

5worldcat.org

5^th place

1medlineplus.gov

1,581^st place

1,299^th place

1oup.com

485^th place

440^th place

1neurologyindia.com

low place

1sciencedirect.com

149^th place

178^th place

doi.org

Clancy, Robert R.; Kelts, K.Alan; Oehlert, John W. (1980). "Clinical variability in congenital fiber type disproportion". Journal of the Neurological Sciences. 46 (3). Elsevier BV: 257–266. doi:10.1016/0022-510x(80)90050-7. ISSN 0022-510X. Retrieved November 21, 2023.
Clarke NF, North KN (October 2003). "Congenital fiber type dispropsortion—30 years on". J. Neuropathol. Exp. Neurol. 62 (10): 977–89. doi:10.1093/jnen/62.10.977. PMID 14575234. Retrieved November 20, 2023.
Na SJ, Kim WK, Kim TS, Kang SW, Lee EY, Choi YC (August 2006). "Comparison of clinical characteristics between congenital fiber type disproportion myopathy and congenital myopathy with type 1 fiber predominance". Yonsei Med. J. 47 (4): 513–8. doi:10.3349/ymj.2006.47.4.513. PMC 2687732. PMID 16941741.
Clarke, Nigel F.; Kolski, Hanna; Dye, Danielle E.; Lim, Esther; Smith, Robert L. L.; Patel, Rakesh; Fahey, Michael C.; Bellance, Rémi; Romero, Norma B.; Johnson, Edward S.; Labarre‐Vila, Annick; Monnier, Nicole; Laing, Nigel G.; North, Kathryn N. (2008). "Mutations in TPM3 are a common cause of congenital fiber type disproportion". Annals of Neurology. 63 (3). Wiley: 329–337. doi:10.1002/ana.21308. ISSN 0364-5134. Retrieved November 20, 2023.
Sobrido, M. J.; Fernández, J. M.; Fontoira, E.; Pérez-Sousa, C.; Cabello, A.; Castro, M.; Teijeira, S.; Álvarez, S.; Mederer, S.; Rivas, E.; Seijo-Martínez, M.; Navarro, C. (April 27, 2005). "Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large family". Brain. 128 (7). Oxford University Press (OUP): 1716–1727. doi:10.1093/brain/awh511. ISSN 1460-2156.
Clarke, Nigel F. (2011). "Congenital Fiber-Type Disproportion". Seminars in Pediatric Neurology. 18 (4). Elsevier BV: 264–271. doi:10.1016/j.spen.2011.10.008. ISSN 1071-9091. Retrieved November 21, 2023.
Clarke, Nigel F.; Waddell, Leigh B.; Cooper, Sandra T.; Perry, Margaret; Smith, Robert L.L.; Kornberg, Andrew J.; Muntoni, Francesco; Lillis, Suzanne; Straub, Volker; Bushby, Kate; Guglieri, Michela; King, Mary D.; Farrell, Michael A.; Marty, Isabelle; Lunardi, Joel; Monnier, Nicole; North, Kathryn N. (May 11, 2010). "Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion". Human Mutation. 31 (7). Hindawi Limited: E1544–E1550. doi:10.1002/humu.21278. ISSN 1059-7794. Retrieved November 21, 2023.

medlineplus.gov

"Congenital fiber-type disproportion: MedlinePlus Genetics". MedlinePlus. May 1, 2016. Retrieved November 21, 2023.

neurologyindia.com

Sharma MC, Ralte AM, Atri SK, Gulati S, Kalra V, Sarkar C (June 2004). "Congenital fiber type disproportion: a rare type of congenital myopathy: a report of four cases". Neurol India. 52 (2): 254–6. PMID 15269486. Retrieved November 20, 2023.

nih.gov

pubmed.ncbi.nlm.nih.gov

Clancy, Robert R.; Kelts, K.Alan; Oehlert, John W. (1980). "Clinical variability in congenital fiber type disproportion". Journal of the Neurological Sciences. 46 (3). Elsevier BV: 257–266. doi:10.1016/0022-510x(80)90050-7. ISSN 0022-510X. Retrieved November 21, 2023.
Clarke NF, North KN (October 2003). "Congenital fiber type dispropsortion—30 years on". J. Neuropathol. Exp. Neurol. 62 (10): 977–89. doi:10.1093/jnen/62.10.977. PMID 14575234. Retrieved November 20, 2023.
Na SJ, Kim WK, Kim TS, Kang SW, Lee EY, Choi YC (August 2006). "Comparison of clinical characteristics between congenital fiber type disproportion myopathy and congenital myopathy with type 1 fiber predominance". Yonsei Med. J. 47 (4): 513–8. doi:10.3349/ymj.2006.47.4.513. PMC 2687732. PMID 16941741.
Clarke, Nigel F.; Kolski, Hanna; Dye, Danielle E.; Lim, Esther; Smith, Robert L. L.; Patel, Rakesh; Fahey, Michael C.; Bellance, Rémi; Romero, Norma B.; Johnson, Edward S.; Labarre‐Vila, Annick; Monnier, Nicole; Laing, Nigel G.; North, Kathryn N. (2008). "Mutations in TPM3 are a common cause of congenital fiber type disproportion". Annals of Neurology. 63 (3). Wiley: 329–337. doi:10.1002/ana.21308. ISSN 0364-5134. Retrieved November 20, 2023.
Sharma MC, Ralte AM, Atri SK, Gulati S, Kalra V, Sarkar C (June 2004). "Congenital fiber type disproportion: a rare type of congenital myopathy: a report of four cases". Neurol India. 52 (2): 254–6. PMID 15269486. Retrieved November 20, 2023.
Clarke, Nigel F.; Waddell, Leigh B.; Cooper, Sandra T.; Perry, Margaret; Smith, Robert L.L.; Kornberg, Andrew J.; Muntoni, Francesco; Lillis, Suzanne; Straub, Volker; Bushby, Kate; Guglieri, Michela; King, Mary D.; Farrell, Michael A.; Marty, Isabelle; Lunardi, Joel; Monnier, Nicole; North, Kathryn N. (May 11, 2010). "Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion". Human Mutation. 31 (7). Hindawi Limited: E1544–E1550. doi:10.1002/humu.21278. ISSN 1059-7794. Retrieved November 21, 2023.

ncbi.nlm.nih.gov

Na SJ, Kim WK, Kim TS, Kang SW, Lee EY, Choi YC (August 2006). "Comparison of clinical characteristics between congenital fiber type disproportion myopathy and congenital myopathy with type 1 fiber predominance". Yonsei Med. J. 47 (4): 513–8. doi:10.3349/ymj.2006.47.4.513. PMC 2687732. PMID 16941741.

oup.com

academic.oup.com

Clarke NF, North KN (October 2003). "Congenital fiber type dispropsortion—30 years on". J. Neuropathol. Exp. Neurol. 62 (10): 977–89. doi:10.1093/jnen/62.10.977. PMID 14575234. Retrieved November 20, 2023.

sciencedirect.com

Clarke, Nigel F. (2011). "Congenital Fiber-Type Disproportion". Seminars in Pediatric Neurology. 18 (4). Elsevier BV: 264–271. doi:10.1016/j.spen.2011.10.008. ISSN 1071-9091. Retrieved November 21, 2023.

worldcat.org

Clancy, Robert R.; Kelts, K.Alan; Oehlert, John W. (1980). "Clinical variability in congenital fiber type disproportion". Journal of the Neurological Sciences. 46 (3). Elsevier BV: 257–266. doi:10.1016/0022-510x(80)90050-7. ISSN 0022-510X. Retrieved November 21, 2023.
Clarke, Nigel F.; Kolski, Hanna; Dye, Danielle E.; Lim, Esther; Smith, Robert L. L.; Patel, Rakesh; Fahey, Michael C.; Bellance, Rémi; Romero, Norma B.; Johnson, Edward S.; Labarre‐Vila, Annick; Monnier, Nicole; Laing, Nigel G.; North, Kathryn N. (2008). "Mutations in TPM3 are a common cause of congenital fiber type disproportion". Annals of Neurology. 63 (3). Wiley: 329–337. doi:10.1002/ana.21308. ISSN 0364-5134. Retrieved November 20, 2023.
Sobrido, M. J.; Fernández, J. M.; Fontoira, E.; Pérez-Sousa, C.; Cabello, A.; Castro, M.; Teijeira, S.; Álvarez, S.; Mederer, S.; Rivas, E.; Seijo-Martínez, M.; Navarro, C. (April 27, 2005). "Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large family". Brain. 128 (7). Oxford University Press (OUP): 1716–1727. doi:10.1093/brain/awh511. ISSN 1460-2156.
Clarke, Nigel F. (2011). "Congenital Fiber-Type Disproportion". Seminars in Pediatric Neurology. 18 (4). Elsevier BV: 264–271. doi:10.1016/j.spen.2011.10.008. ISSN 1071-9091. Retrieved November 21, 2023.
Clarke, Nigel F.; Waddell, Leigh B.; Cooper, Sandra T.; Perry, Margaret; Smith, Robert L.L.; Kornberg, Andrew J.; Muntoni, Francesco; Lillis, Suzanne; Straub, Volker; Bushby, Kate; Guglieri, Michela; King, Mary D.; Farrell, Michael A.; Marty, Isabelle; Lunardi, Joel; Monnier, Nicole; North, Kathryn N. (May 11, 2010). "Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion". Human Mutation. 31 (7). Hindawi Limited: E1544–E1550. doi:10.1002/humu.21278. ISSN 1059-7794. Retrieved November 21, 2023.