Federico A - Search Results

1

Oral self-mutilation in a patient with rhombencephalosynapsys.

Verri A, Uggetti C, Vallero E, Ceroni M, Federico A. Verri A, et al. Among authors: federico a. J Intellect Disabil Res. 2000 Feb;44 ( Pt 1):86-90. doi: 10.1046/j.1365-2788.2000.00242.x. J Intellect Disabil Res. 2000. PMID: 10711654 Review.

2

Late diagnosis in severe and mild intellectual disability in adulthood.

Verri AP, Maraschio P, Uggetti C, Pucci E, Ronchi G, Nespoli L, Destefani V, Ramponi A, Federico A. Verri AP, et al. Among authors: federico a. J Intellect Disabil Res. 2004 Oct;48(Pt 7):679-86. doi: 10.1111/j.1365-2788.2003.00593.x. J Intellect Disabil Res. 2004. PMID: 15357688

3

Chromosome 10p deletion in a patient with hypoparathyroidism, severe mental retardation, autism and basal ganglia calcifications.

Verri A, Maraschio P, Devriendt K, Uggetti C, Spadoni E, Haeusler E, Federico A. Verri A, et al. Among authors: federico a. Ann Genet. 2004 Jul-Sep;47(3):281-7. doi: 10.1016/j.anngen.2004.03.001. Ann Genet. 2004. PMID: 15337474

4

Early/late-life adversities and behavioural phenotypes: insight into metabolomics, genomics and connectomics.

Federico A, Verri A, de Vries PJ. Federico A, et al. J Intellect Disabil Res. 2016 Sep;60(9):833-4. doi: 10.1111/jir.12326. J Intellect Disabil Res. 2016. PMID: 27528383 No abstract available.

5

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

6

Cerebellar dysgenesis and mental retardation associated with a complex chromosome rearrangement.

Maserati E, Verri A, Seghezzi L, Tupler R, Federico A, Tiepolo L, Maraschio P. Maserati E, et al. Among authors: federico a. Ann Genet. 1999;42(4):210-4. Ann Genet. 1999. PMID: 10674160

7

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

8

Cerebellar arteriovenous malformation and vertebral artery aneurysm in a CADASIL patient.

Pescini F, Sarti C, Pantoni L, Mangiafico S, Bianchi S, Dotti MT, Federico A, Inzitari D. Pescini F, et al. Among authors: federico a. Acta Neurol Scand. 2006 Jan;113(1):62-3. doi: 10.1111/j.1600-0404.2005.00539.x. Acta Neurol Scand. 2006. PMID: 16367901

9

Can untreated PKU patients escape from intellectual disability? A systematic review.

van Vliet D, van Wegberg AMJ, Ahring K, Bik-Multanowski M, Blau N, Bulut FD, Casas K, Didycz B, Djordjevic M, Federico A, Feillet F, Gizewska M, Gramer G, Hertecant JL, Hollak CEM, Jørgensen JV, Karall D, Landau Y, Leuzzi V, Mathisen P, Moseley K, Mungan NÖ, Nardecchia F, Õunap K, Powell KK, Ramachandran R, Rutsch F, Setoodeh A, Stojiljkovic M, Trefz FK, Usurelu N, Wilson C, van Karnebeek CD, Hanley WB, van Spronsen FJ. van Vliet D, et al. Among authors: federico a. Orphanet J Rare Dis. 2018 Aug 29;13(1):149. doi: 10.1186/s13023-018-0890-7. Orphanet J Rare Dis. 2018. PMID: 30157945 Free PMC article.

10

Association of trisomy 9p and band heterotopia.

Federico A, Tomasetti P, Zollino M, Diomedi M, Dotti MT, De Stefano N, Gualdi GF, Neri G, Gigli GL. Federico A, et al. Neurology. 1999 Jul 22;53(2):430-2. doi: 10.1212/wnl.53.2.430. Neurology. 1999. PMID: 10430446

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