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Academic Journal

Lung cancer prediction in Lambert-Eaton myasthenic syndrome in a prospective cohort.

Authors : Maddison, Paul¹ ; Lipka, Alexander F.^2,3; Gozzard, Paul⁴

Source: Scientific Reports. 6/29/2020, Vol. 10 Issue 1, p1-5. 5p.

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Academic Journal

Long‐term prognosis of Japanese Lambert–Eaton myasthenic syndrome patients with or without small‐cell lung carcinoma.

Authors : Kojima, Yuta^1,2 (AUTHOR); Uzawa, Akiyuki¹ (AUTHOR) ; Shibuya, Kazumoto¹ (AUTHOR)

Source: Clinical & Experimental Neuroimmunology. May2020, Vol. 11 Issue 2, p131-134. 4p.

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Academic Journal

Miastenija ir Lambert-Eaton miasteninis sindromas, jų gydymo rekomendacijos ir ypatumai COVID-19 pandemijos metu.

Authors : Klimašauskienė, A.¹ ; Bunevičiūtė, R.²

Source: Neurologijos Seminarai. 2020, Vol. 24 Issue 2, p138-144. 7p.

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First maternal uniparental disomy for chromosome 2 with PREPL novel frameshift mutation of congenital myasthenic syndrome 22 in an infant.

Authors : Zhang, Ping^1,2 (AUTHOR); Wu, Bingbing^1,2 (AUTHOR); Lu, Yulan^1,2 (AUTHOR)

Source: Molecular Genetics & Genomic Medicine. Mar2020, Vol. 8 Issue 3, p1-6. 6p.

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Academic Journal

Successful treatment of advanced lung adenocarcinoma complicated with Lambert‐Eaton myasthenic syndrome: A case report and literature review.

Authors : Wang, Aili¹ (AUTHOR) ; Zhang, Xin² (AUTHOR); Yi, Jiawen³ (AUTHOR)

Source: Thoracic Cancer. May2020, Vol. 11 Issue 5, p1334-1338. 5p.

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Academic Journal

Anti‐SOX1 antibody‐positive paraneoplastic neurological syndrome presenting with Lambert‐Eaton myasthenic syndrome and small cell lung cancer: A case report.

Authors : Li, Chunyang¹ (AUTHOR); Wang, Xiaolei² (AUTHOR); Sun, Lihua¹ (AUTHOR)

Source: Thoracic Cancer. Feb2020, Vol. 11 Issue 2, p465-469. 5p.

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A spontaneous missense mutation in the chromodomain helicase DNA‐binding protein 8 (CHD8) gene: a novel association with congenital myasthenic syndrome.

Authors : Lee, C. Y.^1,2 (AUTHOR); Petkova, M.^1,2 (AUTHOR); Morales‐Gonzalez, S.^1,2 (AUTHOR)

Source: Neuropathology & Applied Neurobiology. Oct2020, Vol. 46 Issue 6, p588-601. 14p.

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A case report of an intermediate phenotype between congenital myasthenic syndrome and D-2- and L-2-hydroxyglutaric aciduria due to novel SLC25A1 variants.

Authors : Li, Wenhui¹ (AUTHOR); Zhang, Min¹ (AUTHOR); Zhang, Linmei¹ (AUTHOR)

Source: BMC Neurology. 7/13/2020, Vol. 20 Issue 1, p1-7. 7p. 2 Diagrams, 1 Chart.

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GRP78 antibodies are associated with blood–brain barrier breakdown in paraneoplastic cerebellar degeneration in Lambert‐Eaton myasthenic syndrome.

Authors : Shimizu, Fumitaka¹ (AUTHOR) ; Kanda, Takashi¹ (AUTHOR)

Source: Clinical & Experimental Neuroimmunology. May2020, Vol. 11 Issue 2, p88-89. 2p.

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Non-small cell lung cancer associated with late-onset Lambert-Eaton myasthenic syndrome and paraneoplastic cerebellar degeneration.

Authors : Cai, Guoxin¹ (AUTHOR); Sun, Xindong¹ (AUTHOR); Yu, Jinming¹ (AUTHOR)

Source: Neurological Sciences. May2020, Vol. 41 Issue 5, p1277-1279. 3p. 1 Color Photograph, 1 Black and White Photograph.

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فلترة النتائج

Lung cancer prediction in Lambert-Eaton myasthenic syndrome in a prospective cohort.

Long‐term prognosis of Japanese Lambert–Eaton myasthenic syndrome patients with or without small‐cell lung carcinoma.

Miastenija ir Lambert-Eaton miasteninis sindromas, jų gydymo rekomendacijos ir ypatumai COVID-19 pandemijos metu.

First maternal uniparental disomy for chromosome 2 with PREPL novel frameshift mutation of congenital myasthenic syndrome 22 in an infant.

Successful treatment of advanced lung adenocarcinoma complicated with Lambert‐Eaton myasthenic syndrome: A case report and literature review.

Anti‐SOX1 antibody‐positive paraneoplastic neurological syndrome presenting with Lambert‐Eaton myasthenic syndrome and small cell lung cancer: A case report.

A spontaneous missense mutation in the chromodomain helicase DNA‐binding protein 8 (CHD8) gene: a novel association with congenital myasthenic syndrome.

A case report of an intermediate phenotype between congenital myasthenic syndrome and D-2- and L-2-hydroxyglutaric aciduria due to novel SLC25A1 variants.

GRP78 antibodies are associated with blood–brain barrier breakdown in paraneoplastic cerebellar degeneration in Lambert‐Eaton myasthenic syndrome.

Non-small cell lung cancer associated with late-onset Lambert-Eaton myasthenic syndrome and paraneoplastic cerebellar degeneration.

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