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9. Necessity of Intracranial Imaging in Infants and Children With Macrocephaly. Sampson MA; Berg AD; Huber JN; Olgun G Pediatr Neurol; 2019 Apr; 93():21-26. PubMed ID: 30704866 [TBL] [Abstract][Full Text] [Related]
10. [Developmental outcome of fetal macrocephaly and associated syndromes]. Biran-Gol Y; Lerman-Sagie T; Lev D; Malinger G; Schweiger A; Davidovitch M Harefuah; 2010 Jan; 149(1):41-4, 62, 61. PubMed ID: 20422840 [TBL] [Abstract][Full Text] [Related]
11. Macrocephaly in infancy: benign enlargement of the subarachnoid spaces and subdural collections. Tucker J; Choudhary AK; Piatt J J Neurosurg Pediatr; 2016 Jul; 18(1):16-20. PubMed ID: 26942270 [TBL] [Abstract][Full Text] [Related]
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13. Clinical pitfalls in the diagnosis of segmental overgrowth syndromes: a child with the c.2740G > A mutation in PIK3CA gene. Maguolo A; Antoniazzi F; Spano A; Fiorini E; Gaudino R; Mauro M; Cantalupo G; Biban P; Maitz S; Cavarzere P Ital J Pediatr; 2018 Sep; 44(1):110. PubMed ID: 30231930 [TBL] [Abstract][Full Text] [Related]
14. Megalencephaly, polymicrogyria and ribbon-like band heterotopia: A new cortical malformation. Kobayashi Y; Magara S; Okazaki K; Komatsubara T; Saitsu H; Matsumoto N; Kato M; Tohyama J Brain Dev; 2016 Nov; 38(10):950-953. PubMed ID: 27381655 [TBL] [Abstract][Full Text] [Related]
15. Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly. Alcantara D; Timms AE; Gripp K; Baker L; Park K; Collins S; Cheng C; Stewart F; Mehta SG; Saggar A; Sztriha L; Zombor M; Caluseriu O; Mesterman R; Van Allen MI; Jacquinet A; Ygberg S; Bernstein JA; Wenger AM; Guturu H; Bejerano G; Gomez-Ospina N; Lehman A; Alfei E; Pantaleoni C; Conti V; Guerrini R; Moog U; Graham JM; Hevner R; Dobyns WB; O'Driscoll M; Mirzaa GM Brain; 2017 Oct; 140(10):2610-2622. PubMed ID: 28969385 [TBL] [Abstract][Full Text] [Related]
16. A child with macrocephaly: case report of a patient with megalencephalic leukoencephalopathy with subcortical cysts and a compound heterozygosity for two mutations in the MLC1 gene. Delmonaco AG; Gaidolfi E; Scheper GC; Girardo E; Molinatto C; Belligni E; Ferrero GB; Cirillo Silengo M; Van Der Knaap M Minerva Pediatr; 2011 Apr; 63(2):125-9. PubMed ID: 21487377 [TBL] [Abstract][Full Text] [Related]
17. Heterozygosity for Nuclear Factor One X in mice models features of Malan syndrome. Oishi S; Harkins D; Kurniawan ND; Kasherman M; Harris L; Zalucki O; Gronostajski RM; Burne THJ; Piper M EBioMedicine; 2019 Jan; 39():388-400. PubMed ID: 30503862 [TBL] [Abstract][Full Text] [Related]
18. Magnetic resonance imaging characteristics of benign macrocephaly in children. Alper G; Ekinci G; Yilmaz Y; Arikan C; Telyar G; Erzen C J Child Neurol; 1999 Oct; 14(10):678-82. PubMed ID: 10511342 [TBL] [Abstract][Full Text] [Related]
19. [Megalencephaly: a report of 4 children including a previously undescribed congenital syndrome and review of the literature (author's transl)]. Hoshino A No To Shinkei; 1981 Apr; 33(4):377-84. PubMed ID: 6167278 [TBL] [Abstract][Full Text] [Related]