PubMed

Partial trisomy 13q22-qter associated to leukoencephalopathy and late onset generalised epilepsy.

Ribacoba R, Menendez-Gonzalez M, Hernando I, Salas J, Giros ML.

Int Arch Med. 2008 Apr 29;1(1):5.PMID: 18471271 [PubMed - in process]Related articlesFree article

Simultaneous partial monosomy 5p and trisomy 10q.

Elbistan M.

Indian J Pediatr. 2004 Nov;71(11):1041.PMID: 15572834 [PubMed - in process]Related articles

Partial trisomy of the distal part of 10q: a report of two Egyptian cases.

Aglan MS, Kamel AK, Helmy NA.

Genet Couns. 2008;19(2):199-209.PMID: 18618995 [PubMed - indexed for MEDLINE]Related articles

[Post-stroke epilepsy]

Temprano T, Salas-Puig J, Calleja-Puerta S, Zanabili Al-Sibbai AA, Lahoz CH.

Rev Neurol. 2009 Feb 16-28;48(4):171-7. Spanish. PMID: 19226483 [PubMed - indexed for MEDLINE]Related articlesFree article

A 14-year follow-up of a case detected prenatally of partial trisomy 13q21.32-qter and monosomy 18q22.3-qter as a result of a maternal complex chromosome rearrangement involving chromosomes 6, 13, and 18.

Quadrelli R, Quadrelli A, Milunsky A, Zou YS, Huang XL, Viera E, Mechoso B, Bellini S, Costabel M, Vaglio A.

Genet Test Mol Biomarkers. 2009 Jun;13(3):387-93.PMID: 19473082 [PubMed - indexed for MEDLINE]Related articles

Phylloid hypomelanosis and mosaic partial trisomy 13: two cases that provide further evidence of a distinct clinicogenetic entity.

González-Enseñat MA, Vicente A, Poo P, Catalá V, Mar Pérez-Iribarne M, Fuster C, Geán E, Happle R.

Arch Dermatol. 2009 May;145(5):576-8.PMID: 19451503 [PubMed - indexed for MEDLINE]Related articles

A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.

Peeters H, Vermeesch J, Fryns JP.

Genet Couns. 2008;19(4):365-71.PMID: 19239079 [PubMed - indexed for MEDLINE]Related articles

Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 --> qter) detected in an autistic boy.

Carreira IM, Melo JB, Rodrigues C, Backx L, Vermeesch J, Weise A, Kosyakova N, Oliveira G, Matoso E.

Mol Cytogenet. 2009 Aug 4;2:16.PMID: 19653912 [PubMed - in process]Related articlesFree article

Subtle familial translocation t(11;22)(q24.2;q13.33) resulting in Jacobsen syndrome and distal trisomy 22q13.3: further details of genotype-phenotype maps.

Jamsheer A, Smyk M, Wierzba J, Kołowska J, Woźniak A, Skołozdrzy J, Fischer M, Latos-Bieleńska A.

J Appl Genet. 2008;49(4):397-405.PMID: 19029687 [PubMed - indexed for MEDLINE]Related articlesFree article

Early-onset form of benign childhood epilepsy with centro-temporal EEG foci--a different nosological perspective from Panayiotopoulos syndrome.

Ohtsu M, Oguni H, Imai K, Funatsuka M, Osawa M.

Neuropediatrics. 2008 Feb;39(1):14-9.PMID: 18504676 [PubMed - indexed for MEDLINE]Related articles

Single seizure and epilepsy in patients with a cerebral territorial infarct.

De Reuck J, De Groote L, Van Maele G.

J Neurol Sci. 2008 Aug 15;271(1-2):127-30. Epub 2008 May 20.PMID: 18495161 [PubMed - indexed for MEDLINE]Related articles

Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report.

Aktas D, Weise A, Utine E, Alehan D, Mrasek K, von Eggeling F, Thieme H, Tuncbilek E, Liehr T.

Mol Cytogenet. 2009 Jun 30;2:14.PMID: 19566937 [PubMed - in process]Related articlesFree article

When to start drug treatment for childhood epilepsy: the clinical-epidemiological evidence.

Arts WF, Geerts AT.

Eur J Paediatr Neurol. 2009 Mar;13(2):93-101. Epub 2008 Jun 24. Review.PMID: 18567515 [PubMed - indexed for MEDLINE]Related articles

Trisomy 12p and monosomy 4p: phenotype-genotype correlation.

Benussi DG, Costa P, Zollino M, Murdolo M, Petix V, Carrozzi M, Pecile V.

Genet Test Mol Biomarkers. 2009 Apr;13(2):199-204.PMID: 19378504 [PubMed - indexed for MEDLINE]Related articles

Lennox-Gastaut syndrome with late-onset and prominent reflex seizures in trisomy 21 patients.

Ferlazzo E, Adjien CK, Guerrini R, Calarese T, Crespel A, Elia M, Striano P, Gelisse P, Bramanti P, di Bella P, Genton P.

Epilepsia. 2009 Jun;50(6):1587-95. Epub 2009 Jan 31.PMID: 19187280 [PubMed - indexed for MEDLINE]Related articles

Ictal asystole--late manifestation of partial epilepsy and importance of cardiac pacemaker.

Zubair S, Arshad AB, Saeed B, Luqman S, Oommen KJ.

Seizure. 2009 Jul;18(6):457-61. Epub 2009 May 2.PMID: 19414273 [PubMed - indexed for MEDLINE]Related articles

Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations.

Passemard S, Titomanlio L, Elmaleh M, Afenjar A, Alessandri JL, Andria G, de Villemeur TB, Boespflug-Tanguy O, Burglen L, Del Giudice E, Guimiot F, Hyon C, Isidor B, Mégarbané A, Moog U, Odent S, Hernandez K, Pouvreau N, Scala I, Schaer M, Gressens P, Gerard B, Verloes A.

Neurology. 2009 Sep 22;73(12):962-9.PMID: 19770472 [PubMed - indexed for MEDLINE]Related articles

Distal trisomy of 10q with distal monosomy of 15q due to a paternal translocation.

Sun SC, Luo FW, Song HW, He JB, Peng YS.

J Int Med Res. 2009 Jul-Aug;37(4):1230-7.PMID: 19761709 [PubMed - indexed for MEDLINE]Related articles

Partial trisomy 19p13.3 and partial monosomy 1p36.3: Clinical report and a literature review.

Puvabanditsin S, Garrow E, Brandsma E, Savla J, Kunjumon B, Gadi I.

Am J Med Genet A. 2009 Aug;149A(8):1782-5. Review.PMID: 19610110 [PubMed - indexed for MEDLINE]Related articles

Seizures in childhood ischemic stroke in Taiwan.

Lee JC, Lin KL, Wang HS, Chou ML, Hung PC, Hsieh MY, Lee YY, Lin JJ, Wong AM.

Brain Dev. 2009 Apr;31(4):294-9. Epub 2008 Jul 22.PMID: 18650041 [PubMed - indexed for MEDLINE]Related articles