Federico A - Search Results

1

Association of myopathy with multiple exostoses and mental retardation: a case report.

De Stefano N, Dotti MT, Malandrini A, Federico A. De Stefano N, et al. Among authors: federico a. Brain Dev. 1994 Mar-Apr;16(2):136-8. doi: 10.1016/0387-7604(94)90050-7. Brain Dev. 1994. PMID: 8048702

2

Motor-sensory neuropathy without minifascicles in a patient with 46XY gonadal dysgenesis.

Malandrini A, Gambelli S, Muglia M, Berti G, Gaudiano C, Patitucci A, Sugie K, Umehara F, Quattrone A, Dotti MT, Federico A. Malandrini A, et al. Among authors: federico a. Brain Dev. 2008 Apr;30(4):291-4. doi: 10.1016/j.braindev.2007.07.010. Epub 2007 Sep 4. Brain Dev. 2008. PMID: 17768021

3

Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrum.

Grosso S, Carluccio MA, Cardaioli E, Cerase A, Malandrini A, Romano C, Federico A, Dotti MT. Grosso S, et al. Among authors: federico a. Brain Dev. 2017 Mar;39(3):261-265. doi: 10.1016/j.braindev.2016.09.013. Epub 2016 Oct 11. Brain Dev. 2017. PMID: 27742419

4

Mitochondrial dysfunction in Rett syndrome. An ultrastructural and biochemical study.

Dotti MT, Manneschi L, Malandrini A, De Stefano N, Caznerale F, Federico A. Dotti MT, et al. Among authors: federico a. Brain Dev. 1993 Mar-Apr;15(2):103-6. doi: 10.1016/0387-7604(93)90045-a. Brain Dev. 1993. PMID: 8214327

5

Mental retardation with marfanoid syndrome: presentation of a family with different phenotypical expression.

Dotti MT, Malandrini A, Bartolini S, Fabrizi GM, Federico A. Dotti MT, et al. Among authors: federico a. Brain Dev. 1993 Jul-Aug;15(4):291-4. doi: 10.1016/0387-7604(93)90026-5. Brain Dev. 1993. PMID: 8250152

6

Merosin positive congenital muscular dystrophy with severe involvement of the central nervous system.

De Stefano N, Dotti MT, Villanova M, Scarano G, Federico A. De Stefano N, et al. Among authors: federico a. Brain Dev. 1996 Jul-Aug;18(4):323-6. doi: 10.1016/0387-7604(96)00029-0. Brain Dev. 1996. PMID: 8879654

7

Clinical and stabilometric monitoring in a case of cerebellar atrophy with vitamin E deficiency.

Battisti C, Toffola ED, Verri AP, Serra E, Dotti MT, Formichi P, Federico A. Battisti C, et al. Among authors: federico a. Brain Dev. 1998 Jun;20(4):253-7. doi: 10.1016/s0387-7604(98)00026-6. Brain Dev. 1998. PMID: 9661973

8

A Rett syndrome MECP2 mutation that causes mental retardation in men.

Dotti MT, Orrico A, De Stefano N, Battisti C, Sicurelli F, Severi S, Lam CW, Galli L, Sorrentino V, Federico A. Dotti MT, et al. Among authors: federico a. Neurology. 2002 Jan 22;58(2):226-30. doi: 10.1212/wnl.58.2.226. Neurology. 2002. PMID: 11805248

9

MR evidence of structural and metabolic changes in brains of patients with Werner's syndrome.

De Stefano N, Dotti MT, Battisti C, Sicurelli F, Stromillo ML, Mortilla M, Federico A. De Stefano N, et al. Among authors: federico a. J Neurol. 2003 Oct;250(10):1169-73. doi: 10.1007/s00415-003-0167-4. J Neurol. 2003. PMID: 14586596

10

Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Rufa A, De Stefano N, Dotti MT, Bianchi S, Sicurelli F, Stromillo ML, D'Aniello B, Federico A. Rufa A, et al. Among authors: federico a. Arch Neurol. 2004 Apr;61(4):577-80. doi: 10.1001/archneur.61.4.577. Arch Neurol. 2004. PMID: 15096408

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