Angelina Maria Martins Lino
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Explore the profile of Angelina Maria Martins Lino including associated specialties, affiliations and a list of published articles.
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17
Citations
352
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Recent Articles
1.
Da Silva Teixeira W, Baima J, Lino A
Pract Neurol
. 2024 Sep;
25(1):51-55.
PMID: 39237146
While acute and monophasic diabetic neuropathy variants are considered relatively uncommon, diabetes mellitus affects over 6% of the global population, with more than 50% experiencing some form of diabetic neuropathy....
2.
Baima J, Silva B, Vieira V, Meireles L, Arai M, Lino A
Autops Case Rep
. 2024 Jul;
14:e2024493.
PMID: 39021464
HIV infection is a chameleon, mimicking several diseases. Herein, we report a previously healthy 39-year-old woman who, over 2 months, developed arthritis, weight loss, and confluent multiple mononeuropathy. Extensive laboratory...
3.
Baima J, Moreira A, Lino A
Neurol Sci
. 2023 Feb;
44(5):1831-1832.
PMID: 36781565
A 43-year-old male patient with a 7-year history of liver transplantation due to p.Val50Met hereditary transthyretin amyloidosis (ATTRv) persisted with refractory neuropathic pain, distal weakness, and progressive worsening of dysautonomia....
4.
Szor R, Fernandes F, Lino A, Mendonca L, Seguro F, Feitosa V, et al.
Orphanet J Rare Dis
. 2022 Dec;
17(1):425.
PMID: 36471404
Background: Systemic amyloidosis is caused by the deposition of misfolded protein aggregates in tissues, leading to progressive organ dysfunction and death. Epidemiological studies originate predominantly from high-income countries, with few...
5.
Fernandes F, de Alencar Neto A, Kerges Bueno B, Fonseca Cafezeiro C, Rissato J, Szor R, et al.
Arq Bras Cardiol
. 2022 Mar;
118(2):422-432.
PMID: 35262576
Background: Systemic amyloidosis is a disease with heterogeneous clinical manifestations. Diagnosis depends on clinical suspicion combined with specific complementary methods. Objective: To describe the clinical, laboratory, electrocardiographic, and imaging profile...
6.
Diagnostic challenges in systemic amyloidosis: a case report with clinical and laboratorial pitfalls
Lino A, Castelli J, Szor R, Fernandes F, Aiello V
Autops Case Rep
. 2021 Oct;
11:e2021326.
PMID: 34631606
Currently, there is growing evidence in the literature warning of misdiagnosis involving amyloidosis and chronic inflammatory demyelinating polyneuropathy (CIDP). Although inducing clinical manifestations outside the peripheral nervous system, light chain...
7.
de Oliveira A, Taranto P, Herbst L, Kirihara A, Veras M, Serafim Silva A, et al.
Autops Case Rep
. 2019 Sep;
3(1):53-61.
PMID: 31528598
Known since the 19th century, neuromyelitis optica (NMO), or Devic's disease, is an idiopathic immune-mediated inflammatory demyelinating disease of the central nervous system selectively affecting the optic nerve and spinal...
8.
Lino A, Spera R, de Campos F, Freitas C, Garcia M, da Costa Lopes L, et al.
Autops Case Rep
. 2017 Jun;
4(1):29-37.
PMID: 28652990
Described in 1962, the opsoclonus-myoclonus-ataxia syndrome (OMAS) is a rare, neurologically debilitating disorder with distinct characteristics that may begin in childhood or adult life. Although many cases remain without etiological...
9.
Sato D, Callegaro D, Lana-Peixoto M, Waters P, de Haidar Jorge F, Takahashi T, et al.
Neurology
. 2014 Jan;
82(6):474-81.
PMID: 24415568
Objective: To evaluate clinical features among patients with neuromyelitis optica spectrum disorders (NMOSD) who have myelin oligodendrocyte glycoprotein (MOG) antibodies, aquaporin-4 (AQP4) antibodies, or seronegativity for both antibodies. Methods: Sera...
10.