Ignatius J - Search Results

1

Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment.

Guerreiro MM, Andermann E, Guerrini R, Dobyns WB, Kuzniecky R, Silver K, Van Bogaert P, Gillain C, David P, Ambrosetto G, Rosati A, Bartolomei F, Parmeggiani A, Paetau R, Salonen O, Ignatius J, Borgatti R, Zucca C, Bastos AC, Palmini A, Fernandes W, Montenegro MA, Cendes F, Andermann F. Guerreiro MM, et al. Among authors: ignatius j. Ann Neurol. 2000 Jul;48(1):39-48. Ann Neurol. 2000. PMID: 10894214

2

Electromagnetic function of polymicrogyric cortex in congenital bilateral perisylvian syndrome.

Paetau R, Saraneva J, Salonen O, Valanne L, Ignatius J, Salenius S. Paetau R, et al. Among authors: ignatius j. J Neurol Neurosurg Psychiatry. 2004 May;75(5):717-22. doi: 10.1136/jnnp.2002.004754. J Neurol Neurosurg Psychiatry. 2004. PMID: 15090566 Free PMC article.

3

Sodium Channel SCN3A (Na_V1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development.

Smith RS, Kenny CJ, Ganesh V, Jang A, Borges-Monroy R, Partlow JN, Hill RS, Shin T, Chen AY, Doan RN, Anttonen AK, Ignatius J, Medne L, Bönnemann CG, Hecht JL, Salonen O, Barkovich AJ, Poduri A, Wilke M, de Wit MCY, Mancini GMS, Sztriha L, Im K, Amrom D, Andermann E, Paetau R, Lehesjoki AE, Walsh CA, Lehtinen MK. Smith RS, et al. Among authors: ignatius j. Neuron. 2018 Sep 5;99(5):905-913.e7. doi: 10.1016/j.neuron.2018.07.052. Epub 2018 Aug 23. Neuron. 2018. PMID: 30146301 Free PMC article.

4

De novo paracentric inversion 14q13q24.1 in a patient with severe involuntary movements, epilepsy, oligodontia and dysmorphic features.

Peippo M, Tengström C, Arvio M, Valanne L, Oksanen V, Kaakkola S, Ignatius J. Peippo M, et al. Among authors: ignatius j. Genet Couns. 2004;15(3):341-6. Genet Couns. 2004. PMID: 15517827

5

Pitt-Hopkins syndrome in two patients and further definition of the phenotype.

Peippo MM, Simola KO, Valanne LK, Larsen AT, Kähkönen M, Auranen MP, Ignatius J. Peippo MM, et al. Among authors: ignatius j. Clin Dysmorphol. 2006 Apr;15(2):47-54. doi: 10.1097/01.mcd.0000184973.14775.32. Clin Dysmorphol. 2006. PMID: 16531728

6

Weismann-Netter syndrome and mental retardation: a new patient and review of the literature.

Peippo M, Valanne L, Perhomaa M, Toivanen L, Ignatius J. Peippo M, et al. Among authors: ignatius j. Am J Med Genet A. 2009 Nov;149A(11):2593-601. doi: 10.1002/ajmg.a.33019. Am J Med Genet A. 2009. PMID: 19839038 Review.

7

[Current prospects of genetics in epilepsy diagnostics--when and what?].

Uusimaa J, Gaily E, Ignatius J, Lehesjoki AE. Uusimaa J, et al. Among authors: ignatius j. Duodecim. 2009;125(22):2521-30. Duodecim. 2009. PMID: 20095121 Review. Finnish.

8

Hydrolethalus syndrome: neuropathology of 21 cases confirmed by HYLS1 gene mutation analysis.

Paetau A, Honkala H, Salonen R, Ignatius J, Kestilä M, Herva R. Paetau A, et al. Among authors: ignatius j. J Neuropathol Exp Neurol. 2008 Aug;67(8):750-62. doi: 10.1097/NEN.0b013e318180ec2e. J Neuropathol Exp Neurol. 2008. PMID: 18648327

9

Calvarial doughnut lesions and osteoporosis: a new three-generation family and review.

Jaakkola E, Laine CM, Mäyränpää MK, Falck A, Ignatius J, Mäkitie O. Jaakkola E, et al. Among authors: ignatius j. Am J Med Genet A. 2009 Nov;149A(11):2371-7. doi: 10.1002/ajmg.a.33040. Am J Med Genet A. 2009. PMID: 19839042 Review.

10

Smith-Lemli-Opitz syndrome and other sterol disorders among Finns with developmental disabilities.

Nissinen MJ, Gylling H, Kaski M, Tammisto P, Mieskonen S, Ignatius J, Miettinen TA. Nissinen MJ, et al. Among authors: ignatius j. J Lab Clin Med. 2000 Dec;136(6):457-67. doi: 10.1067/mlc.2000.110607. J Lab Clin Med. 2000. PMID: 11128747

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