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Bilateral Combined Hamartoma of the Retina and Retinal Pigment Epithelium in Neurofibromatosis Type 2.
J Neuroophthalmol. 2022 Dec 1;42(4):e591-e592. doi: 10.1097/WNO.0000000000001557. Epub 2022 Apr 27.
J Neuroophthalmol. 2022.
PMID: 35483063
No abstract available.
DNM1L mutation presenting as progressive myoclonic epilepsy associated with acute febrile infection-related epilepsy syndrome.
De Souza Crippa AC, Franklin GL, Takeshita BT, Ghizoni Teive HA.
De Souza Crippa AC, et al.
Epileptic Disord. 2022 Oct 1;24(5):976-978. doi: 10.1684/epd.2022.1474.
Epileptic Disord. 2022.
PMID: 35894675
Free article.
English.
No abstract available.
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Abnormal Findings in Polysomnographic Recordings of Patients with Spinocerebellar Ataxia Type 2 (SCA2).
Zanatta A, Camargo CHF, Germiniani FMB, Raskin S, de Souza Crippa AC, Teive HAG.
Zanatta A, et al. Among authors: de souza crippa ac.
Cerebellum. 2019 Apr;18(2):196-202. doi: 10.1007/s12311-018-0982-x.
Cerebellum. 2019.
PMID: 30264264
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The relationship between gross motor function impairment in cerebral palsy and sleeping issues of children and caregivers.
Obrecht A, Fischer de Almeida M, Maltauro L, Leite da Silva WD, Bueno Zonta M, de Souza Crippa AC.
Obrecht A, et al. Among authors: de souza crippa ac.
Sleep Med. 2021 May;81:261-267. doi: 10.1016/j.sleep.2021.02.055. Epub 2021 Mar 4.
Sleep Med. 2021.
PMID: 33743473
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