Claudia Suemi Kamoi Kay
Overview
Explore the profile of Claudia Suemi Kamoi Kay including associated specialties, affiliations and a list of published articles.
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53
Citations
203
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Recent Articles
1.
Lorenzoni P, Filla L, Dal-Pra Ducci R, Fustes O, Raquel do Vale Pascoal Rodrigues P, Arndt R, et al.
Neurol Sci
. 2024 Oct;
46(2):1019-1022.
PMID: 39477909
We report a 9-year-old girl with delayed motor milestones and respiratory difficulty since birth. She presented as a floppy infant, with generalised muscle wasting, dysphagia and facial weakness. The muscle...
2.
Lorenzoni P, Suemi Kamoi Kay C, Dal-Pra Ducci R, Fustes O, Raquel do Vale Pascoal Rodrigues P, Arndt R, et al.
Arq Neuropsiquiatr
. 2024 Feb;
82(2):1-4.
PMID: 38395422
Carnitine palmitoyltransferase II (CPT II) deficiency is an autosomal recessive inherited disorder related to lipid metabolism affecting skeletal muscle. The first cases of CPT II deficiency causing myopathy were reported...
3.
Raquel do Vale Pascoal Rodrigues P, Suemi Kamoi Kay C, Dal-Pra Ducci R, Utiumi M, Fustes O, Werneck L, et al.
Arq Neuropsiquiatr
. 2024 Feb;
82(1):1-7.
PMID: 38316426
Background: (MG) is an autoimmune disease usually caused by antibodies against the acetylcholine receptor (AChR-Abs), muscle-specific tyrosine kinase (MuSK-Abs), or low-density lipoprotein receptor-related protein 4 (LRP4-Abs). However, there are MG...
4.
Lorenzoni P, Suemi Kamoi Kay C, Dal-Pra Ducci R, Fustes O, Raquel do Vale Pascoal Rodrigues P, Hrysay N, et al.
Arq Neuropsiquiatr
. 2023 Oct;
81(10):922-933.
PMID: 37852290
Limb-girdle muscular dystrophy (LGMD) is a group of myopathies that lead to progressive muscle weakness, predominantly involving the shoulder and pelvic girdles; it has a heterogeneous genetic etiology, with variation...
5.
Lorenzoni P, Bayer D, Dal-Pra Ducci R, Fustes O, Raquel do Vale Pascoal Rodrigues P, Werneck L, et al.
Neurol Sci
. 2023 Mar;
44(7):2551-2554.
PMID: 36964315
We report a patient with early-onset hereditary sensory and autonomic neuropathy type 1A (HSAN-1A) who developed a distinct phenotype, with tongue fasciculation and atrophy, due to a mutation at serine...
6.
Lorenzoni P, Giugno V, Dal-Pra Ducci R, Werneck L, Suemi Kamoi Kay C, Scola R
Acta Neurol Belg
. 2023 Feb;
123(4):1655-1657.
PMID: 36840806
No abstract available.
7.
Fustes O, Suemi Kamoi Kay C, Lorenzoni P, Dal-Pra Ducci R, Ribas M, Werneck L, et al.
Arq Neuropsiquiatr
. 2022 Apr;
80(5):545.
PMID: 35476077
No abstract available.
8.
Lorenzoni P, Dal-Pra Ducci R, Arndt R, Hrysay N, Fustes O, Topf A, et al.
Arq Neuropsiquiatr
. 2021 Dec;
80(1):69-74.
PMID: 34932651
Background: Congenital myasthenic syndromes (CMS) have some phenotypic overlap with seronegative myasthenia gravis (SNMG). Objective: The aim of this single center study was to assess the minimum occurrence of CMS...
9.
Fustes O, Suemi Kamoi Kay C, Lorenzoni P, Dal-Pra Ducci R, Werneck L, Scola R
Arq Neuropsiquiatr
. 2021 Dec;
80(2):208-210.
PMID: 34932646
In 1951, the physiologist George Duncan Dawson presented his work with the averaging of the signal in the evoked potentials (EPs), opening a new stage in the development of clinical...
10.
Dal-Pra Ducci R, Tessaro C, Suemi Kamoi Kay C, Fustes O, Werneck L, Lorenzoni P, et al.
Arq Neuropsiquiatr
. 2021 Nov;
80(3):270-279.
PMID: 34816968
Background: Polyneuropathies are characterized by a symmetrical impairment of the peripheral nervous system, resulting in sensory, motor and/or autonomic deficits. Due to the heterogeneity of causes, an etiological diagnosis for...