A case of juvenile CLN1– challenge in diagnosis and epilepsy treatment-Reference-Cited by-同舟云学术

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A case of juvenile CLN1– challenge in diagnosis and epilepsy treatment

Published:2021-03-04 Issue:2 Volume:27 Page:165-168
ISSN:1355-4794
Container-title:Neurocase
language:en
Short-container-title:Neurocase

Author:

Kravljanac Ruzica¹²^ORCID,Sims Katherine³

Affiliation:

1. Faculty for Medicine, University of Belgrade, Belgrade, Serbia

2. Neurology Department, Institute for Mother and Child Healthcare of Serbia, Belgrade, Serbia

3. Neurology Department, Massachusetts General Hospital, Harvard Medical School, Boston, USA

Publisher

Informa UK Limited

Subject

Neurology (clinical),Arts and Humanities (miscellaneous)

Link

https://www.tandfonline.com/doi/pdf/10.1080/13554794.2021.1905852

Reference14 articles.

1. Human pathology in NCL

2. Progressive conduction defects and cardiac death in late infantile neuronal ceroid lipofuscinosis

3. Late onset juvenile neuronal ceroid-lipofuscinosis with granular osmiophilic deposits (GROD)

4. Considering Valproate as a Risk Factor for Rapid Exacerbation of Complex Movement Disorder in Progressed Stages of Late-Infantile CLN2 Disease

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1. GABA_AR-PPT1 palmitoylation homeostasis controls synaptic transmission and circuitry oscillation in CLN1 disease;2024-03-29

2. Levetiracetam;Reactions Weekly;2021-05

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