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Engel, Andrew

Mayo Clinic

Mayo Clinic

Citations 11

Muscle Biopsy and Electromyography Correlation (P3.442)
Milone, Margherita , Litchy, William J. , Mandrekar, Jayawant, Engel, Andrew, Naddaf, Elie , Mauermann, Michelle L.

Neurology | December 7, 2023 | Volume: 90 | Issue: 15_supplement | Pages: No page available

10.1212/wnl.90.15_supplement.p3.442 Get It

Undiagnosed Congenital Myasthenic Syndromes in Adult Neuromuscular Practice: a Long Road to Diagnosis and Treatment. (P2.033)
Kao, Justin, Milone, Margherita , Selcen, Duygu , Shen, Xin‐Ming , Engel, Andrew, Liewluck, Teerin

Neurology | December 7, 2023 | Volume: 90 | Issue: 15_supplement | Pages: No page available

10.1212/wnl.90.15_supplement.p2.033 Get It

Congenital Myasthenic Syndromes (CMS) Due to Impaired Principal Coupling Pathway in the ɛ Subunit of Muscle Acetylcholine Receptor (AChR) (P2.031)
Shen, Xin‐Ming , Brengman, Joan M., Shen, Shelley , Durmuş, Hacer , Deymeer, Feza , Sine, Steven M. , Engel, Andrew, Preethish‐Kumar, Veeramani , Yüceyar, Nur , Vengalil, Seena , Nalini, Atchayaram

Neurology | December 7, 2023 | Volume: 90 | Issue: 15_supplement | Pages: No page available

10.1212/wnl.90.15_supplement.p2.031 Get It

Determinants of the Repetitive-CMAP Occurrence and Therapy Efficacy in Slow-Channel Myasthenia (1253)
Di, Li , Chen, Hai , Selcen, Duygu , Engel, Andrew, Da, Yuwei , Shen, Xin‐Ming , Di, Li, Lü, Yan

Neurology | December 7, 2023 | Volume: 96 | Issue: 15_supplement | Pages: No page available

10.1212/wnl.96.15_supplement.1253 Get It

Distinctive pathological features of inherited and sporadic late-onset nemaline myopathies (2368)
Selcen, Duygu , Engel, Andrew, Milone, Margherita , Nicolau, Stefan , Dasgupta, Aneesha , Doles, Jason D.

Neurology | December 7, 2023 | Volume: 94 | Issue: 15_supplement | Pages: No page available

10.1212/wnl.94.15_supplement.2368 Get It

A Spontaneously Resolving Pyridostigmine Responsive Congenital Myasthenic Syndrome Caused by Isolated PREPL Deficiency (S45.004)
Selcen, Duygu , Shen, Xin , Meulemans, Sandra, Creemers, John W.M. , Engel, Andrew, Régal, Luc

Neurology | December 7, 2023 | Volume: 80 | Issue: 7_supplement | Pages: No page available

10.1212/wnl.80.7_supplement.s45.004 Get It

A Spontaneously Resolving Pyridostigmine Responsive Congenital Myasthenic Syndrome Caused by Isolated PREPL Deficiency (IN1-1.001)
Selcen, Duygu , Shen, Xin , Meulemans, Sandra, Creemers, John W.M. , Engel, Andrew, Régal, Luc

Neurology | December 7, 2023 | Volume: 80 | Issue: 7_supplement | Pages: No page available

10.1212/wnl.80.7_supplement.in1-1.001 Get It

A new muscle glycogen storage disease associated with Glycogenin-1 deficiency (S34.002)
Hedberg‐Oldfors, Carola , Hernández‐Laín, Aurelio , Viennet, G., Michel, Fabrice , Ackman, Hasan, Kornblum, Cornelia , Romero, Norma B., Engel, Andrew, DiMauro, Salvatore, Malfatti, Edoardo , Nilsson, Johanna E. , Domínguez‐González, Cristina , Michel, Fabrice, Bergh, Peter Y. K. Van den , Romero, Norma B. , Oldfors, Anders

Neurology | December 6, 2023 | Volume: 84 | Issue: 14_supplement | Pages: No page available

10.1212/wnl.84.14_supplement.s34.002 Get It

A quantitative analysis of muscle microvasculature in areas of perifascicular fiber atrophy (PFA) and adjacent unaffected fascicular areas (UFA) in dermatomyositis (DM). (S17.001)
Lahoria, Rajat , Engel, Andrew

Neurology | December 6, 2023 | Volume: 84 | Issue: 14_supplement | Pages: No page available

10.1212/wnl.84.14_supplement.s17.001 Get It

Congenital myasthenic syndrome (CMS) caused by novel mutation in LRP4. Phenotypic heterogeneity and defects in neuromuscular transmission (NMT) identified in a second kinship (P2.021)
Selcen, Duygu , Shen, Xin‐Ming , McEvoy, Kathleen M., Engel, Andrew, Ohkawara, Bisei , Ohno, Kinji

Neurology | December 6, 2023 | Volume: 84 | Issue: 14_supplement | Pages: No page available

10.1212/wnl.84.14_supplement.p2.021 Get It