Neuromuscular junction (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Neuromuscular junction" in English language version.

refsWebsite

Global rank English rank

27nih.gov

4^th place

17doi.org

2^nd place

7semanticscholar.org

11^th place

8^th place

3web.archive.org

1^st place

2harvard.edu

18^th place

17^th place

1handle.net

102^nd place

76^th place

1mda.org

low place

1raredr.com

low place

1fda.gov

447^th place

338^th place

doi.org

Rygiel KA, Picard M, Turnbull DM (August 2016). "The ageing neuromuscular system and sarcopenia: a mitochondrial perspective". The Journal of Physiology. 594 (16): 4499–4512. doi:10.1113/JP271212. PMC 4983621. PMID 26921061.
Sine SM (July 2012). "End-plate acetylcholine receptor: structure, mechanism, pharmacology, and disease". Physiological Reviews. 92 (3): 1189–1234. doi:10.1152/physrev.00015.2011. PMC 3489064. PMID 22811427.
Van der Kloot W, Molgó J (October 1994). "Quantal acetylcholine release at the vertebrate neuromuscular junction". Physiological Reviews. 74 (4): 899–991. doi:10.1152/physrev.1994.74.4.899. PMID 7938228.
Scuka M, Mozrzymas JW (1992). "Postsynaptic potentiation and desensitization at the vertebrate end-plate receptors". Progress in Neurobiology. 38 (1): 19–33. doi:10.1016/0301-0082(92)90033-B. PMID 1736323. S2CID 38497982.
Valenzuela DM, Stitt TN, DiStefano PS, Rojas E, Mattsson K, Compton DL, et al. (September 1995). "Receptor tyrosine kinase specific for the skeletal muscle lineage: expression in embryonic muscle, at the neuromuscular junction, and after injury". Neuron. 15 (3): 573–584. doi:10.1016/0896-6273(95)90146-9. PMID 7546737. S2CID 17575761.
Glass DJ, Bowen DC, Stitt TN, Radziejewski C, Bruno J, Ryan TE, et al. (May 1996). "Agrin acts via a MuSK receptor complex". Cell. 85 (4): 513–523. doi:10.1016/S0092-8674(00)81252-0. PMID 8653787. S2CID 14930468.
Witzemann V (November 2006). "Development of the neuromuscular junction". Cell and Tissue Research. 326 (2): 263–271. doi:10.1007/s00441-006-0237-x. hdl:11858/00-001M-0000-002B-BE74-A. PMID 16819627. S2CID 30829665.
Okada K, Inoue A, Okada M, Murata Y, Kakuta S, Jigami T, et al. (June 2006). "The muscle protein Dok-7 is essential for neuromuscular synaptogenesis". Science. 312 (5781): 1802–1805. Bibcode:2006Sci...312.1802O. doi:10.1126/science.1127142. PMID 16794080. S2CID 45730054.
Steinbeck JA, Jaiswal MK, Calder EL, Kishinevsky S, Weishaupt A, Toyka KV, et al. (January 2016). "Functional Connectivity under Optogenetic Control Allows Modeling of Human Neuromuscular Disease". Cell Stem Cell. 18 (1): 134–143. doi:10.1016/j.stem.2015.10.002. PMC 4707991. PMID 26549107.
Papapetropoulos S, Singer C (April 2007). "Botulinum toxin in movement disorders". Seminars in Neurology. 27 (2): 183–194. doi:10.1055/s-2007-971171. PMID 17390263.
Lewis RL, Gutmann L (June 2004). "Snake venoms and the neuromuscular junction". Seminars in Neurology. 24 (2): 175–179. doi:10.1055/s-2004-830904. PMID 15257514.
Finsterer J, Papić L, Auer-Grumbach M (October 2011). "Motor neuron, nerve, and neuromuscular junction disease". Current Opinion in Neurology. 24 (5): 469–474. doi:10.1097/WCO.0b013e32834a9448. PMID 21825986.
Luigetti M, Modoni A, Lo Monaco M (April 2013). "Low rate repetitive nerve stimulation in Lambert-Eaton myasthenic syndrome: peculiar characteristics of decremental pattern from a single-centre experience". Clinical Neurophysiology. 124 (4): 825–826. doi:10.1016/j.clinph.2012.08.026. PMID 23036181. S2CID 11396376.
Titulaer MJ, Lang B, Verschuuren JJ (December 2011). "Lambert-Eaton myasthenic syndrome: from clinical characteristics to therapeutic strategies". The Lancet. Neurology. 10 (12): 1098–1107. doi:10.1016/S1474-4422(11)70245-9. PMID 22094130. S2CID 27421424.
Harper CM (March 2004). "Congenital myasthenic syndromes". Seminars in Neurology. 24 (1): 111–123. doi:10.1055/s-2004-829592. PMID 15229798.
Engel AG, Shen XM, Selcen D, Sine SM (April 2015). "Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment". The Lancet. Neurology. 14 (4): 420–434. doi:10.1016/S1474-4422(14)70201-7. PMC 4520251. PMID 25792100.
Engel AG, Shen XM, Selcen D, Sine S (December 2012). "New horizons for congenital myasthenic syndromes". Annals of the New York Academy of Sciences. 1275 (1): 54–62. Bibcode:2012NYASA1275...54E. doi:10.1111/j.1749-6632.2012.06803.x. PMC 3546605. PMID 23278578.

fda.gov

accessdata.fda.gov

"Amifampridine phosphate for the treatment of congenital myasthenic syndromes". FDA orphan drug designation. U.S. Food and Drug Administration. Archived from the original on 26 July 2015.

handle.net

hdl.handle.net

Witzemann V (November 2006). "Development of the neuromuscular junction". Cell and Tissue Research. 326 (2): 263–271. doi:10.1007/s00441-006-0237-x. hdl:11858/00-001M-0000-002B-BE74-A. PMID 16819627. S2CID 30829665.

harvard.edu

ui.adsabs.harvard.edu

Okada K, Inoue A, Okada M, Murata Y, Kakuta S, Jigami T, et al. (June 2006). "The muscle protein Dok-7 is essential for neuromuscular synaptogenesis". Science. 312 (5781): 1802–1805. Bibcode:2006Sci...312.1802O. doi:10.1126/science.1127142. PMID 16794080. S2CID 45730054.
Engel AG, Shen XM, Selcen D, Sine S (December 2012). "New horizons for congenital myasthenic syndromes". Annals of the New York Academy of Sciences. 1275 (1): 54–62. Bibcode:2012NYASA1275...54E. doi:10.1111/j.1749-6632.2012.06803.x. PMC 3546605. PMID 23278578.

mda.org

"LEMS: Firdapse Study Shows Encouraging Results". Muscular Dystrophy Association Press Release. Archived from the original on 10 November 2015.

nih.gov

pubmed.ncbi.nlm.nih.gov

Jimsheleishvili S, Marwaha K, Sherman AL (2024), "Physiology, Neuromuscular Transmission", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 31082177, retrieved 2024-08-26
Rygiel KA, Picard M, Turnbull DM (August 2016). "The ageing neuromuscular system and sarcopenia: a mitochondrial perspective". The Journal of Physiology. 594 (16): 4499–4512. doi:10.1113/JP271212. PMC 4983621. PMID 26921061.
Sine SM (July 2012). "End-plate acetylcholine receptor: structure, mechanism, pharmacology, and disease". Physiological Reviews. 92 (3): 1189–1234. doi:10.1152/physrev.00015.2011. PMC 3489064. PMID 22811427.
Van der Kloot W, Molgó J (October 1994). "Quantal acetylcholine release at the vertebrate neuromuscular junction". Physiological Reviews. 74 (4): 899–991. doi:10.1152/physrev.1994.74.4.899. PMID 7938228.
Scuka M, Mozrzymas JW (1992). "Postsynaptic potentiation and desensitization at the vertebrate end-plate receptors". Progress in Neurobiology. 38 (1): 19–33. doi:10.1016/0301-0082(92)90033-B. PMID 1736323. S2CID 38497982.
Valenzuela DM, Stitt TN, DiStefano PS, Rojas E, Mattsson K, Compton DL, et al. (September 1995). "Receptor tyrosine kinase specific for the skeletal muscle lineage: expression in embryonic muscle, at the neuromuscular junction, and after injury". Neuron. 15 (3): 573–584. doi:10.1016/0896-6273(95)90146-9. PMID 7546737. S2CID 17575761.
Glass DJ, Bowen DC, Stitt TN, Radziejewski C, Bruno J, Ryan TE, et al. (May 1996). "Agrin acts via a MuSK receptor complex". Cell. 85 (4): 513–523. doi:10.1016/S0092-8674(00)81252-0. PMID 8653787. S2CID 14930468.
Witzemann V (November 2006). "Development of the neuromuscular junction". Cell and Tissue Research. 326 (2): 263–271. doi:10.1007/s00441-006-0237-x. hdl:11858/00-001M-0000-002B-BE74-A. PMID 16819627. S2CID 30829665.
Okada K, Inoue A, Okada M, Murata Y, Kakuta S, Jigami T, et al. (June 2006). "The muscle protein Dok-7 is essential for neuromuscular synaptogenesis". Science. 312 (5781): 1802–1805. Bibcode:2006Sci...312.1802O. doi:10.1126/science.1127142. PMID 16794080. S2CID 45730054.
Steinbeck JA, Jaiswal MK, Calder EL, Kishinevsky S, Weishaupt A, Toyka KV, et al. (January 2016). "Functional Connectivity under Optogenetic Control Allows Modeling of Human Neuromuscular Disease". Cell Stem Cell. 18 (1): 134–143. doi:10.1016/j.stem.2015.10.002. PMC 4707991. PMID 26549107.
Papapetropoulos S, Singer C (April 2007). "Botulinum toxin in movement disorders". Seminars in Neurology. 27 (2): 183–194. doi:10.1055/s-2007-971171. PMID 17390263.
Lewis RL, Gutmann L (June 2004). "Snake venoms and the neuromuscular junction". Seminars in Neurology. 24 (2): 175–179. doi:10.1055/s-2004-830904. PMID 15257514.
Finsterer J, Papić L, Auer-Grumbach M (October 2011). "Motor neuron, nerve, and neuromuscular junction disease". Current Opinion in Neurology. 24 (5): 469–474. doi:10.1097/WCO.0b013e32834a9448. PMID 21825986.
Newsom-Davis J (July 2007). "The emerging diversity of neuromuscular junction disorders". Acta Myologica. 26 (1): 5–10. PMC 2949330. PMID 17915563.
Bardhan M, Dogra H, Samanta D (2021). "Neonatal Myasthenia Gravis". StatPearls. StatPearls. PMID 32644361.
Luigetti M, Modoni A, Lo Monaco M (April 2013). "Low rate repetitive nerve stimulation in Lambert-Eaton myasthenic syndrome: peculiar characteristics of decremental pattern from a single-centre experience". Clinical Neurophysiology. 124 (4): 825–826. doi:10.1016/j.clinph.2012.08.026. PMID 23036181. S2CID 11396376.
Titulaer MJ, Lang B, Verschuuren JJ (December 2011). "Lambert-Eaton myasthenic syndrome: from clinical characteristics to therapeutic strategies". The Lancet. Neurology. 10 (12): 1098–1107. doi:10.1016/S1474-4422(11)70245-9. PMID 22094130. S2CID 27421424.
Harper CM (March 2004). "Congenital myasthenic syndromes". Seminars in Neurology. 24 (1): 111–123. doi:10.1055/s-2004-829592. PMID 15229798.
Engel AG, Shen XM, Selcen D, Sine SM (April 2015). "Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment". The Lancet. Neurology. 14 (4): 420–434. doi:10.1016/S1474-4422(14)70201-7. PMC 4520251. PMID 25792100.
Engel AG, Shen XM, Selcen D, Sine S (December 2012). "New horizons for congenital myasthenic syndromes". Annals of the New York Academy of Sciences. 1275 (1): 54–62. Bibcode:2012NYASA1275...54E. doi:10.1111/j.1749-6632.2012.06803.x. PMC 3546605. PMID 23278578.

ncbi.nlm.nih.gov

Rygiel KA, Picard M, Turnbull DM (August 2016). "The ageing neuromuscular system and sarcopenia: a mitochondrial perspective". The Journal of Physiology. 594 (16): 4499–4512. doi:10.1113/JP271212. PMC 4983621. PMID 26921061.
Sine SM (July 2012). "End-plate acetylcholine receptor: structure, mechanism, pharmacology, and disease". Physiological Reviews. 92 (3): 1189–1234. doi:10.1152/physrev.00015.2011. PMC 3489064. PMID 22811427.
Steinbeck JA, Jaiswal MK, Calder EL, Kishinevsky S, Weishaupt A, Toyka KV, et al. (January 2016). "Functional Connectivity under Optogenetic Control Allows Modeling of Human Neuromuscular Disease". Cell Stem Cell. 18 (1): 134–143. doi:10.1016/j.stem.2015.10.002. PMC 4707991. PMID 26549107.
Newsom-Davis J (July 2007). "The emerging diversity of neuromuscular junction disorders". Acta Myologica. 26 (1): 5–10. PMC 2949330. PMID 17915563.
Bardhan M, Dogra H, Samanta D (2021). "Neonatal Myasthenia Gravis". StatPearls. StatPearls. PMID 32644361.
Engel AG, Shen XM, Selcen D, Sine SM (April 2015). "Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment". The Lancet. Neurology. 14 (4): 420–434. doi:10.1016/S1474-4422(14)70201-7. PMC 4520251. PMID 25792100.
Engel AG, Shen XM, Selcen D, Sine S (December 2012). "New horizons for congenital myasthenic syndromes". Annals of the New York Academy of Sciences. 1275 (1): 54–62. Bibcode:2012NYASA1275...54E. doi:10.1111/j.1749-6632.2012.06803.x. PMC 3546605. PMID 23278578.

raredr.com

Radke J (30 October 2014). "Catalyst Using the Expanded Access Program to Conduct Phase IV Study with LEMS Patients". Rare Disease Report. Archived from the original on 2015-07-25.

semanticscholar.org

api.semanticscholar.org

Scuka M, Mozrzymas JW (1992). "Postsynaptic potentiation and desensitization at the vertebrate end-plate receptors". Progress in Neurobiology. 38 (1): 19–33. doi:10.1016/0301-0082(92)90033-B. PMID 1736323. S2CID 38497982.
Valenzuela DM, Stitt TN, DiStefano PS, Rojas E, Mattsson K, Compton DL, et al. (September 1995). "Receptor tyrosine kinase specific for the skeletal muscle lineage: expression in embryonic muscle, at the neuromuscular junction, and after injury". Neuron. 15 (3): 573–584. doi:10.1016/0896-6273(95)90146-9. PMID 7546737. S2CID 17575761.
Glass DJ, Bowen DC, Stitt TN, Radziejewski C, Bruno J, Ryan TE, et al. (May 1996). "Agrin acts via a MuSK receptor complex". Cell. 85 (4): 513–523. doi:10.1016/S0092-8674(00)81252-0. PMID 8653787. S2CID 14930468.
Witzemann V (November 2006). "Development of the neuromuscular junction". Cell and Tissue Research. 326 (2): 263–271. doi:10.1007/s00441-006-0237-x. hdl:11858/00-001M-0000-002B-BE74-A. PMID 16819627. S2CID 30829665.
Okada K, Inoue A, Okada M, Murata Y, Kakuta S, Jigami T, et al. (June 2006). "The muscle protein Dok-7 is essential for neuromuscular synaptogenesis". Science. 312 (5781): 1802–1805. Bibcode:2006Sci...312.1802O. doi:10.1126/science.1127142. PMID 16794080. S2CID 45730054.
Luigetti M, Modoni A, Lo Monaco M (April 2013). "Low rate repetitive nerve stimulation in Lambert-Eaton myasthenic syndrome: peculiar characteristics of decremental pattern from a single-centre experience". Clinical Neurophysiology. 124 (4): 825–826. doi:10.1016/j.clinph.2012.08.026. PMID 23036181. S2CID 11396376.
Titulaer MJ, Lang B, Verschuuren JJ (December 2011). "Lambert-Eaton myasthenic syndrome: from clinical characteristics to therapeutic strategies". The Lancet. Neurology. 10 (12): 1098–1107. doi:10.1016/S1474-4422(11)70245-9. PMID 22094130. S2CID 27421424.

web.archive.org

"LEMS: Firdapse Study Shows Encouraging Results". Muscular Dystrophy Association Press Release. Archived from the original on 10 November 2015.
Radke J (30 October 2014). "Catalyst Using the Expanded Access Program to Conduct Phase IV Study with LEMS Patients". Rare Disease Report. Archived from the original on 2015-07-25.
"Amifampridine phosphate for the treatment of congenital myasthenic syndromes". FDA orphan drug designation. U.S. Food and Drug Administration. Archived from the original on 26 July 2015.