P Nicolaides
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Explore the profile of P Nicolaides including associated specialties, affiliations and a list of published articles.
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24
Citations
372
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Recent Articles
1.
Papoulidis I, Kontodiou M, Tzimina M, Saitis I, Hamid A, Klein E, et al.
Cytogenet Genome Res
. 2012 Apr;
136(4):237-41.
PMID: 22487875
Tetrasomy 9p is a rare chromosomal syndrome and about 30% of known cases exhibit mosaicism. Approximately 50 of the reported cases with tetrasomy 9p mosaicism show a characteristic facial appearance,...
2.
Dunkley C, Kung J, Scott R, Nicolaides P, Neville B, Aylett S, et al.
Epilepsy Res
. 2010 Dec;
93(2-3):96-106.
PMID: 21156345
Purpose: Resective epilepsy surgery in early childhood has become an important treatment option for selected infants and children with epilepsy. We describe experience and clinical outcomes of children under 3...
3.
Gore D, Hildebrand G, Sekhri R, Nicolaides P, Leitch J
Eur J Ophthalmol
. 2007 Oct;
17(5):864-6.
PMID: 17932871
Purpose: To report a case of presumed infective meningoencephalitis complicated by bilateral optic neuritis. Methods: Interventional case report. Results: A 7-year-old Pakistani girl presented with fever and multiple right-sided focal...
4.
Adab N, Kini U, Vinten J, Ayres J, Baker G, Clayton-Smith J, et al.
J Neurol Neurosurg Psychiatry
. 2004 Oct;
75(11):1575-83.
PMID: 15491979
Objectives: To determine the prevalence of cognitive delay and possible associated dysmorphic features in children exposed to antiepileptic drugs (AEDs) in utero. Design: Retrospective study of children born to mothers...
5.
Dosios T, Stinios J, Nicolaides P, Spyrakos S, Androulakakis E, Constantopoulos A
Pediatr Surg Int
. 2004 Jun;
20(11-12):863-5.
PMID: 15185105
Pleuropulmonary blastoma (PPB) is an extremely rare intrathoracic neoplasm of early childhood with an unfavorable outcome. In this article, two children with PPB associated with pre-existing pulmonary cysts are presented....
6.
Nicolaides P, Liebsch D, Dale N, Leonard J, Surtees R
Arch Dis Child
. 2002 Jan;
86(1):54-6.
PMID: 11806886
Background: Ornithine carbamoyltransferase (OCT) deficiency is the commonest of the inherited urea cycle disorders. Aims: To determine the long term neurological and cognitive outcome of continuously treated surviving patients. Methods:...
7.
Mohamed K, Appleton R, Nicolaides P
Eur J Paediatr Neurol
. 2000 Oct;
4(5):219-23.
PMID: 11030068
A late diagnosis of Duchenne muscular dystrophy has implications for both child and family. This repeat audit has shown that the diagnosis continues to be delayed. The failure to recognize...
8.
Samantas E, Skarlos D, Pectasides D, Nicolaides P, Kalofonos H, Mylonakis N, et al.
Lung Cancer
. 1999 Apr;
23(2):159-68.
PMID: 10217620
Sixty patients with poor prognostic features, either with extensive disease (ED) or limited disease (LD) small cell lung cancer (SCLC), were treated on an out-patient basis with Carboplatin 80 mg/m2...
9.
Nicolaides P, Leonard J, Surtees R
Arch Dis Child
. 1998 Aug;
78(6):508-12.
PMID: 9713004
Objective: To assess the long term outcome of patients with methylmalonic acidaemia in a cross sectional study. Patients: All 35 patients with methylmalonic acidaemia seen at Great Ormond Street Hospital...
10.
Bugge M, Collins A, Petersen M, Fisher J, Brandt C, Hertz J, et al.
Hum Mol Genet
. 1998 May;
7(4):661-9.
PMID: 9499419
A sample of 100 trisomy 18 conceptuses analysed separately and together with a published sample of 61 conceptuses confirms that an error in maternal meiosis II (MII) is the most...