PMC Articles for MedGen (Select 41946) - PMC

Hidenori Ogata, Xu Zhang, Saeko Inamizu, Ken‐ichiro Yamashita, Ryo Yamasaki, Takuya Matsushita, Noriko Isobe, Akio Hiwatashi, Shozo Tobimatsu, Jun‐ichi Kira

Ann Clin Transl Neurol. 2020 Nov; 7(11): 2297–2309. Published online 2020 Oct 20. doi: 10.1002/acn3.51220

PMCID:: PMC7664262

Abstract Article PDF–2.9M

Select item 108660834.

Facial Neuropathy Revealed: A Case Report on Trigeminal Schwannoma

Emeka Emedike, Azzam Alnughaythir, Naif Alsayed, Ahlam Alharbi, Bader Alotibi

Cureus. 2024 Jan; 16(1): e52302. Published online 2024 Jan 15. doi: 10.7759/cureus.52302

PMCID:: PMC10866083

Abstract Article PDF–791K

Select item 29925085.

Distinctive response of CNS glial cells in oro-facial pain associated with injury, infection and inflammation

SeungHwan Lee, Yuan Qing Zhao, Alfredo Ribeiro-da-Silva, Ji Zhang

Mol Pain. 2010; 6: 79. Published online 2010 Nov 10. doi: 10.1186/1744-8069-6-79

PMCID:: PMC2992508

Abstract Article PDF–21M

Select item 63442516.

Dopamine receptor D2, but not D1, mediates descending dopaminergic pathway-produced analgesic effect in a trigeminal neuropathic pain mouse model

Sufang Liu, Yuanyuan Tang, Hui Shu, Delton Tatum, Qian Bai, Joshua Crawford, Ying Xing, Mary Kay Lobo, Larry Bellinger, Phillip Kramer, Feng Tao

Pain. Author manuscript; available in PMC 2020 Feb 1.

Published in final edited form as: Pain. 2019 Feb; 160(2): 334–344. doi: 10.1097/j.pain.0000000000001414

PMCID:: PMC6344251

Abstract Article PDF–1.2M

Select item 31167227.

Familial Dyskinesia and Facial Myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21

Wendy H. Raskind, Mark Matsushita, Beate Peter, Jeffrey Biberston, John Wolff, Hillary Lipe, Ruben Burbank, Thomas D. Bird

Am J Med Genet B Neuropsychiatr Genet. Author manuscript; available in PMC 2011 Jun 16.

Published in final edited form as: Am J Med Genet B Neuropsychiatr Genet. 2009 Jun 5; 150B(4): 570–574. doi: 10.1002/ajmg.b.30879

PMCID:: PMC3116722

Abstract Article PDF–104K

Select item 31943338.

Congenital innervation dysgenesis syndrome (CID)/congenital cranial dysinnervation disorders (CCDDs)

A A Assaf

Eye (Lond) 2011 Oct; 25(10): 1251–1261. Published online 2011 Jul 1. doi: 10.1038/eye.2011.38

PMCID:: PMC3194333

Abstract Article PDF–591K

Select item 59534149.

A Novel Role for Lymphotactin (XCL1) Signaling in the Nervous System: XCL1 Acts via its Receptor XCR1 to Increase Trigeminal Neuronal Excitability

Emma V. Bird, Tommaso Iannitti, Claire R. Christmas, Ilona Obara, Veselin I. Andreev, Anne E. King, Fiona M. Boissonade

Neuroscience. 2018 May 21; 379: 334–349. doi: 10.1016/j.neuroscience.2018.03.030

PMCID:: PMC5953414

Abstract Article

Select item 592063810.

Infectious Retrovirus Is Inactivated by Serum but Not by Cerebrospinal Fluid or Fluid from Tumor Bed in Patients with Malignant Glioma

Keiji Shimizu, Yasuyoshi Miyao, Masakazu Tamura, Haruhiko Kishima, Motohisa Ohkawa, Eiichiro Mabuchi, Masanobu Yamada, Toru Hayakawa, Kazuhiro Ikenaka

Jpn J Cancer Res. 1995 Nov; 86(11): 1010–1013. doi: 10.1111/j.1349-7006.1995.tb03013.x

PMCID:: PMC5920638

Summary PDF–224K

Select item 584318911.

Identification of STAC3 variants in non-Native American families with overlapping features of Carey-Fineman-Ziter syndrome and Moebius syndrome

Aida Telegrafi, Bryn D. Webb, Sarah M. Robbins, Carlos E. Speck-Martins, David FitzPatrick, Leah Fleming, Richard Redett, Andres Dufke, Gunnar Houge, Jeske J.T. van Harssel, Alain Verloes, Angela Robles, Irini Manoli, Elizabeth C. Engle, Moebius Syndrome Research Consortium, Ethylin Wang Jabs, David Valle, John Carey, Julie E. Hoover-Fong, Nara L.M. Sobreira

Am J Med Genet A. Author manuscript; available in PMC 2018 Oct 1.

Published in final edited form as: Am J Med Genet A. 2017 Oct; 173(10): 2763–2771. Published online 2017 Aug 4. doi: 10.1002/ajmg.a.38375

PMCID:: PMC5843189

Abstract Article PDF–447K

Select item 581913712.

An overlap case of Parry–Romberg syndrome and en coup de sabre with striking ocular involvement and anti-double-stranded DNA positivity

Hatice Ataş, Müzeyyen Gönül, Aysun Gökçe, Mutlu Acar, Canan Gürdal

Indian J Ophthalmol. 2018 Feb; 66(2): 336–338. doi: 10.4103/ijo.IJO_196_17

PMCID:: PMC5819137

Abstract Article PDF–1.0M

Select item 336414013.

Improved Facial Nerve Identification with Novel Fluorescently Labeled Probe

Amy P Wu, Michael A Whitney, Jessica L Crisp, Beth Friedman, Roger Y Tsien, Quyen T Nguyen

Laryngoscope. 2011 Apr; 121(4): 805–810. Published online 2011 Feb 16. doi: 10.1002/lary.21411

PMCID:: PMC3364140

Abstract Article PDF–356K

Select item 568296014.

Defining a mechanistic link between pigment epithelium–derived factor, docosahexaenoic acid, and corneal nerve regeneration

Thang Luong Pham, Jiucheng He, Azucena H. Kakazu, Bokkyoo Jun, Nicolas G. Bazan, Haydee E. P. Bazan

J Biol Chem. 2017 Nov 10; 292(45): 18486–18499. Published online 2017 Sep 26. doi: 10.1074/jbc.M117.801472

PMCID:: PMC5682960

Abstract Article PDF–3.3M

Select item 338474815.

CD4⁺ T cell-mediated neuroprotection is independent of T cell-derived BDNF in a mouse facial nerve axotomy model

Junping Xin, Nichole A. Mesnard, Taylor Beahrs, Derek A. Wainwright, Craig J. Serpe, Thomas D. Alexander, Virginia M. Sanders, Kathryn J. Jones

Brain Behav Immun. Author manuscript; available in PMC 2013 Aug 1.

Published in final edited form as: Brain Behav Immun. 2012 Aug; 26(6): 886–890. Published online 2012 Mar 7. doi: 10.1016/j.bbi.2012.02.011

PMCID:: PMC3384748

Abstract Article PDF–1.5M

Select item 558820716.

Orofacial Granulomatosis: Clinical Signs of Different Pathologies

Giuseppe Troiano, Mario Dioguardi, Giovanni Giannatempo, Luigi Laino, Nunzio Francesco Testa, Roberto Cocchi, Alfredo De Lillo, Lorenzo Lo Muzio

Med Princ Pract. 2015 Feb; 24(2): 117–122. Published online 2015 Jan 9. doi: 10.1159/000369810

PMCID:: PMC5588207

Abstract Article PDF–168K

Select item 339726417.

HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1^−/− Mice

Bryn D. Webb, Sherin Shaaban, Harald Gaspar, Luis F. Cunha, Christian R. Schubert, Ke Hao, Caroline D. Robson, Wai-Man Chan, Caroline Andrews, Sarah MacKinnon, Darren T. Oystreck, David G. Hunter, Anthony J. Iacovelli, Xiaoqian Ye, Anne Camminady, Elizabeth C. Engle, Ethylin Wang Jabs

Am J Hum Genet. 2012 Jul 13; 91(1): 171–179. doi: 10.1016/j.ajhg.2012.05.018

PMCID:: PMC3397264

Abstract Article PDF–726K

Select item 286269318.

HOXA1 mutations are not a common cause of Möbius syndrome

Jessica K. Rankin, Caroline Andrews, Wai-Man Chan, Elizabeth C. Engle

J AAPOS. Author manuscript; available in PMC 2010 Aug 1.

Published in final edited form as: J AAPOS. 2010 Feb; 14(1): 78–80. doi: 10.1016/j.jaapos.2009.11.007

PMCID:: PMC2862693

Abstract Article PDF–28K

Select item 521723619.

Moebius sequence –a multidisciplinary clinical approach

Line Kjeldgaard Pedersen, Rikke Damkjær Maimburg, Jens Michael Hertz, Hans Gjørup, Thomas Klit Pedersen, Bjarne Møller-Madsen, John Rosendahl Østergaard

Orphanet J Rare Dis. 2017; 12: 4. Published online 2017 Jan 6. doi: 10.1186/s13023-016-0559-z

PMCID:: PMC5217236

Abstract Article PDF–3.6M

Select item 637874020.

Chemokines and matrix metalloproteinases in cerebrospinal fluid of patients with central nervous system complications caused by varicella-zoster virus

Liza Lind, Kristina Eriksson, Anna Grahn

J Neuroinflammation. 2019; 16: 42. Published online 2019 Feb 18. doi: 10.1186/s12974-019-1428-1

PMCID:: PMC6378740

Abstract Article PDF–1.1M

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