Papadimitriou A - Search Results

1

Stiff-person like syndrome in a patient with multiple pituitary hormone deficiencies.

Chroni E, Papadimitriou A, Avramidis T, Terentiou AE, Tzioras C, Divari R. Chroni E, et al. Among authors: papadimitriou a. Acta Neurol Scand. 2000 Dec;102(6):403-5. doi: 10.1034/j.1600-0404.2000.102006403.x. Acta Neurol Scand. 2000. PMID: 11125758

2

The influence of Coenzyme Q10 on total serum calcium concentration in two patients with Kearns-Sayre Syndrome and hypoparathyroidism.

Papadimitriou A, Hadjigeorgiou GM, Divari R, Papagalanis N, Comi G, Bresolin N. Papadimitriou A, et al. Neuromuscul Disord. 1996 Jan;6(1):49-53. doi: 10.1016/0960-8966(95)00020-8. Neuromuscul Disord. 1996. PMID: 8845718

3

Continuous muscle fiber activity associated with morphea (localized scleroderma).

Papadimitriou A, Chroni E, Anastasopoulos I, Avramidis T, Hadjigeorgiou G, Koutroumanidis M. Papadimitriou A, et al. Neurology. 1998 Dec;51(6):1763-4. doi: 10.1212/wnl.51.6.1763. Neurology. 1998. PMID: 9855545 No abstract available.

4

Spinal cord compression due to extramedullary haematopoiesis in two patients with thalassaemia: complete regression with blood transfusion therapy.

Aliberti B, Patrikiou A, Terentiou A, Frangatou S, Papadimitriou A. Aliberti B, et al. Among authors: papadimitriou a. J Neurol. 2001 Jan;248(1):18-22. doi: 10.1007/s004150170264. J Neurol. 2001. PMID: 11266014

5

Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome.

Papadimitriou A, Comi GP, Hadjigeorgiou GM, Bordoni A, Sciacco M, Napoli L, Prelle A, Moggio M, Fagiolari G, Bresolin N, Salani S, Anastasopoulos I, Giassakis G, Divari R, Scarlato G. Papadimitriou A, et al. Neurology. 1998 Oct;51(4):1086-92. doi: 10.1212/wnl.51.4.1086. Neurology. 1998. PMID: 9781534

6

McArdle's disease: two clinical expressions in the same pedigree.

Papadimitriou A, Manta P, Divari R, Karabetsos A, Papadimitriou E, Bresolin N. Papadimitriou A, et al. Among authors: papadimitriou e. J Neurol. 1990 Jul;237(4):267-70. doi: 10.1007/BF00314633. J Neurol. 1990. PMID: 2391551

7

Reduced brain stem excitability in mitochondrial myopathy: evidence for early detection with blink reflex habituation studies.

Koutroumanidis M, Papadimitriou A, Bouzas E, Avramidis T, Papathanassopoulos P, Howard RS, Papapetropoulos T. Koutroumanidis M, et al. Among authors: papadimitriou a. Muscle Nerve. 1996 Dec;19(12):1586-95. doi: 10.1002/(SICI)1097-4598(199612)19:12<1586::AID-MUS8>3.0.CO;2-6. Muscle Nerve. 1996. PMID: 8941273

8

A novel missense adenine nucleotide translocator-1 gene mutation in a Greek adPEO family.

Napoli L, Bordoni A, Zeviani M, Hadjigeorgiou GM, Sciacco M, Tiranti V, Terentiou A, Moggio M, Papadimitriou A, Scarlato G, Comi GP. Napoli L, et al. Among authors: papadimitriou a. Neurology. 2001 Dec 26;57(12):2295-8. doi: 10.1212/wnl.57.12.2295. Neurology. 2001. PMID: 11756613

9

L-2-hydroxyglutaric aciduria: two further cases.

Divry P, Jakobs C, Vianey-Saban C, Gibson KM, Michelakakis H, Papadimitriou A, Divari R, Chabrol B, Cournelle MA, Livet MO. Divry P, et al. Among authors: papadimitriou a. J Inherit Metab Dis. 1993;16(3):505-7. doi: 10.1007/BF00711666. J Inherit Metab Dis. 1993. PMID: 7609438 No abstract available.

10

Late onset lipid storage myopathy due to multiple acyl CoA dehydrogenase deficiency triggered by valproate.

Papadimitriou A, Servidei S. Papadimitriou A, et al. Neuromuscul Disord. 1991;1(4):247-52. doi: 10.1016/0960-8966(91)90097-c. Neuromuscul Disord. 1991. PMID: 1822802

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