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Items: 31

1.

Guillain-Barré syndrome with unilateral peripheral facial and bulbar palsy in a child: A case report.

Sharma K, Tengsupakul S, Sanchez O, Phaltas R, Maertens P.

SAGE Open Med Case Rep. 2019 Mar 21;7:2050313X19838750. doi: 10.1177/2050313X19838750. eCollection 2019.

2.

Atypical Cyanotic Breath-Holding Spells in an Infant With 16p11.2 Microdeletion Syndrome.

Bhat J, Martinez J, Maertens P.

Clin Pediatr (Phila). 2018 Mar;57(3):365-367. doi: 10.1177/0009922817717328. Epub 2017 Jun 30. No abstract available.

PMID:
28664753
3.

Infantile Lhermitte-Duclos Disease Treated Successfully With Rapamycin.

Zak M, Ledbetter M, Maertens P.

J Child Neurol. 2017 Mar;32(3):322-326. doi: 10.1177/0883073816681340. Epub 2016 Dec 8.

PMID:
27932596
4.

Intermediate filament protein accumulation in motor neurons derived from giant axonal neuropathy iPSCs rescued by restoration of gigaxonin.

Johnson-Kerner BL, Ahmad FS, Diaz AG, Greene JP, Gray SJ, Samulski RJ, Chung WK, Van Coster R, Maertens P, Noggle SA, Henderson CE, Wichterle H.

Hum Mol Genet. 2015 Mar 1;24(5):1420-31. doi: 10.1093/hmg/ddu556. Epub 2014 Nov 4.

5.

The Shepherd's Crook Sign: A New Neuroimaging Pareidolia in Joubert Syndrome.

Manley AT, Maertens PM.

J Neuroimaging. 2015 May-Jun;25(3):510-2. doi: 10.1111/jon.12159. Epub 2014 Sep 18.

PMID:
25230909
6.

Cerebellar hemorrhage: a major morbidity in extremely preterm infants.

Zayek MM, Benjamin JT, Maertens P, Trimm RF, Lal CV, Eyal FG.

J Perinatol. 2012 Sep;32(9):699-704. doi: 10.1038/jp.2011.185. Epub 2011 Dec 15.

PMID:
22173133
7.

Pediatric gliomatosis cerebri mimicking acute disseminated encephalomyelitis.

Richard HT, Harrison JF, Abel TW, Maertens P, Martino AM, Sosnowski JS.

Pediatrics. 2010 Aug;126(2):e479-82. doi: 10.1542/peds.2009-2303. Epub 2010 Jul 12.

PMID:
20624801
8.

Anti-musk antibody after thymectomy in a previously seropositive myasthenic child.

Saulat B, Maertens P, Hamilton WJ, Bassam BA.

Neurology. 2007 Aug 21;69(8):803-4. No abstract available.

PMID:
17709714
9.

Gene symbol: RPS6KA3.

Chen TJ, Wang Y, Martinez JE, Wilson GL, He XY, Tuck-Muller CM, Maertens P, Wertelecki W, Chen TJ.

Hum Genet. 2007 Apr;121(2):288. No abstract available.

PMID:
17598200
10.

A novel RSK2 (RPS6KA3) gene mutation associated with abnormal brain MRI findings in a family with Coffin-Lowry syndrome.

Wang Y, Martinez JE, Wilson GL, He XY, Tuck-Muller CM, Maertens P, Wertelecki W, Chen TJ.

Am J Med Genet A. 2006 Jun 15;140(12):1274-9.

PMID:
16691578
11.

Cardiofaciocutaneous syndrome (CFC) with congenital peripheral neuropathy and nonorganic malnutrition: an autopsy study.

Manci EA, Martinez JE, Horenstein MG, Gardner TM, Ahmed A, Mancao MC, Gremse DA, Gardner DM, Nimityongskul P, Maertens P, Riddick L, Kavamura MI.

Am J Med Genet A. 2005 Aug 15;137(1):1-8.

PMID:
16007634
12.

Elevated plasma gamma-aminobutyric acid (GABA) levels in autistic youngsters: stimulus for a GABA hypothesis of autism.

Dhossche D, Applegate H, Abraham A, Maertens P, Bland L, Bencsath A, Martinez J.

Med Sci Monit. 2002 Aug;8(8):PR1-6.

PMID:
12165753
13.

Pontine cryptococcoma in a nonimmunocompromised individual: MRI characteristics.

Kesler R, Maertens P.

J Neuroimaging. 1999 Apr;9(2):118-21.

PMID:
10208111
14.

Altered antioxidant enzyme activities in children with a serious adverse experience related to valproic acid therapy.

Graf WD, Oleinik OE, Glauser TA, Maertens P, Eder DN, Pippenger CE.

Neuropediatrics. 1998 Aug;29(4):195-201.

PMID:
9762695
15.

Clinical manifestations of mitochondrial DNA depletion.

Vu TH, Sciacco M, Tanji K, Nichter C, Bonilla E, Chatkupt S, Maertens P, Shanske S, Mendell J, Koenigsberger MR, Sharer L, Schon EA, DiMauro S, DeVivo DC.

Neurology. 1998 Jun;50(6):1783-90.

PMID:
9633728
16.

Mitochondrial encephalopathies.

Maertens P.

Semin Pediatr Neurol. 1996 Dec;3(4):279-97. Review.

PMID:
8969010
17.

Free radicals, anticonvulsants, and the neuronal ceroid-lipofuscinoses.

Maertens P, Dyken P, Graf W, Pippenger C, Chronister R, Shah A.

Am J Med Genet. 1995 Jun 5;57(2):225-8.

PMID:
7668334
18.

Cellular distribution of lesions in Batten disease.

Chronister R, Dyken P, Fields PA, Maertens P.

Am J Med Genet. 1995 Jun 5;57(2):191-5.

PMID:
7668329
19.

Cerebellar infarct: late complication of the Fontan procedure?

Hutto RL, Williams JP, Maertens P, Wilder WM, Williams RS.

Pediatr Neurol. 1991 Jul-Aug;7(4):293-5.

PMID:
1930422
20.

Glutathione peroxidase deficiency and childhood seizures.

Weber GF, Maertens P, Meng XZ, Pippenger CE.

Lancet. 1991 Jun 15;337(8755):1443-4.

PMID:
1675321
21.

Maternal-fetal transport of vitamin K1 and its effects on coagulation in premature infants.

Yang YM, Simon N, Maertens P, Brigham S, Liu P.

J Pediatr. 1989 Dec;115(6):1009-13.

PMID:
2585215
23.

Cell-to-cell communication in peptide target cells of anterior pituitary.

Denef C, Maertens P, Allaerts W, Mignon A, Robberecht W, Swennen L, Carmeliet P.

Methods Enzymol. 1989;168:47-71. No abstract available.

PMID:
2725309
24.

Imaging through the posterior fontanelle.

Maertens P.

J Child Neurol. 1989;4 Suppl:S62-7.

PMID:
2681380
25.

History of the cerebrohepatorenal syndrome of Zellweger and other peroxisomal disorders.

Zellweger H, Maertens P, Superneau D, Wertelecki W.

South Med J. 1988 Mar;81(3):357-64. Review.

PMID:
2450404
26.

A new type of mitochondrial encephalomyopathy with stroke-like episodes due to cytochrome oxidase deficiency.

Maertens P, Richardson R, Bastian F, Williams JP, Hommes F.

J Inherit Metab Dis. 1988;11 Suppl 2:186-8. No abstract available.

PMID:
2846960
27.

Intracranial hemorrhage and cerebral angiopathic changes in a suicidal phenylpropanolamine poisoning.

Maertens P, Lum G, Williams JP, White J.

South Med J. 1987 Dec;80(12):1584-6.

PMID:
3423905
28.
29.

Magnetic resonance imaging of mesial temporal sclerosis: case reports.

Maertens PM, Machen BC, Williams JP, Evans O, Bebin J, Bassam B, Lum GB.

J Comput Tomogr. 1987 Apr;11(2):136-9.

PMID:
3581847
30.

The use of neuropsychological evaluation in the medical management of subdural empyema.

Maertens P, Cohen M, Krawiecki N.

Arch Clin Neuropsychol. 1987;2(2):145-54.

PMID:
14591142
31.

[Long-term diazoxide therapy in recurrent leucine-sensitive hypoglycemia (author's transl)].

Maertens P, de Geeter B, Kurtz F, Messer J, Raber A, Willard D.

Ann Pediatr (Paris). 1980 Dec;27(10):677-81. French. No abstract available.

PMID:
7212555

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