Johansen JG - Search Results

1

Clinical, MRI, and pathological features of polymicrogyria in chromosome 22q11 deletion syndrome.

Sztriha L, Guerrini R, Harding B, Stewart F, Chelloug N, Johansen JG. Sztriha L, et al. Among authors: johansen jg. Am J Med Genet A. 2004 Jun 15;127A(3):313-7. doi: 10.1002/ajmg.a.30014. Am J Med Genet A. 2004. PMID: 15150787

2

Spectrum of malformations of the hindbrain (cerebellum, pons, and medulla) in a cohort of children with high rate of parental consanguinity.

Sztriha L, Johansen JG. Sztriha L, et al. Among authors: johansen jg. Am J Med Genet A. 2005 Jun 1;135(2):134-41. doi: 10.1002/ajmg.a.30701. Am J Med Genet A. 2005. PMID: 15832356

3

Extreme microcephaly with agyria-pachygyria, partial agenesis of the corpus callosum, and pontocerebellar dysplasia.

Sztriha L, Johansen JG, Al-Gazali LI. Sztriha L, et al. Among authors: johansen jg. J Child Neurol. 2005 Feb;20(2):170-2. doi: 10.1177/08830738050200021301. J Child Neurol. 2005. PMID: 15794192

4

Microcephaly associated with abnormal gyral pattern.

Sztriha L, Dawodu A, Gururaj A, Johansen JG. Sztriha L, et al. Among authors: johansen jg. Neuropediatrics. 2004 Dec;35(6):346-52. doi: 10.1055/s-2004-830430. Neuropediatrics. 2004. PMID: 15627942

5

Complex consanguinity associated with short rib-polydactyly syndrome III and congenital infection-like syndrome: a diagnostic problem in dysmorphic syndromes.

al-Gazali LI, Sztriha L, Dawodu A, Varady E, Bakir M, Khdir A, Johansen J. al-Gazali LI, et al. J Med Genet. 1999 Jun;36(6):461-6. J Med Genet. 1999. PMID: 10874634 Free PMC article.

6

Magnetic resonance imaging findings and novel mutations in GM1 gangliosidosis.

Gururaj A, Sztriha L, Hertecant J, Johansen JG, Georgiou T, Campos Y, Drousiotou A, d'Azzo A. Gururaj A, et al. Among authors: johansen jg. J Child Neurol. 2005 Jan;20(1):57-60. doi: 10.1177/08830738050200010901. J Child Neurol. 2005. PMID: 15791924

7

Sturge-Weber syndrome without facial nevus: a case report and review of the literature.

Gururaj AK, Sztriha L, Johansen J, Nork M. Gururaj AK, et al. Acta Paediatr. 2000 Jun;89(6):740-3. doi: 10.1080/080352500750044133. Acta Paediatr. 2000. PMID: 10914976 Review. No abstract available.

8

Frameshift mutation of the zinc finger homeo box 1 B gene in syndromic corpus callosum agenesis (Mowat-Wilson syndrome).

Sztriha L, Espinosa-Parrilla Y, Gururaj A, Amiel J, Lyonnet S, Gerami S, Johansen JG. Sztriha L, et al. Among authors: johansen jg. Neuropediatrics. 2003 Dec;34(6):322-5. doi: 10.1055/s-2003-44671. Neuropediatrics. 2003. PMID: 14681759

9

X-linked hydrocephalus: a novel missense mutation in the L1CAM gene.

Sztriha L, Vos YJ, Verlind E, Johansen J, Berg B. Sztriha L, et al. Pediatr Neurol. 2002 Oct;27(4):293-6. doi: 10.1016/s0887-8994(02)00440-x. Pediatr Neurol. 2002. PMID: 12435569

10

In vivo dosimetry with an inorganic scintillation detector during multi-channel vaginal cylinder pulsed dose-rate brachytherapy: Dosimetry for pulsed dose-rate brachytherapy.

Georgi PD, Nielsen SK, Hansen AT, Spejlborg H, Rylander S, Lindegaard J, Buus S, Wulff C, Petric P, Tanderup K, Johansen JG. Georgi PD, et al. Among authors: johansen jg. Phys Imaging Radiat Oncol. 2024 Aug 25;32:100638. doi: 10.1016/j.phro.2024.100638. eCollection 2024 Oct. Phys Imaging Radiat Oncol. 2024. PMID: 39310220 Free PMC article.

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