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Items: 21

1.

QF-PCR examination of parental and meiotic origin of trisomy 21 in Central and Eastern Europe.

Machatkova M, Brouckova M, Matejckova M, Krebsova A, Sperling K, Vorsanova S, Kutsev S, Zerova T, Arbuzova S, Krejci R, Petersen M, Macek M Sr.

J Histochem Cytochem. 2005 Mar;53(3):371-3.

PMID:
15750023
2.

Low first-trimester pregnancy-associated plasma protein-A and Cornelia de Lange syndrome.

Arbuzova S, Nikolenko M, Krantz D, Hallahan T, Macri J.

Prenat Diagn. 2003 Oct;23(10):864. No abstract available.

PMID:
14558036
3.

Frequency and clinical consequences of extremely high maternal serum PAPP-A levels.

Cuckle H, Arbuzova S, Spencer K, Crossley J, Barkai G, Krantz D, Muller F, Nikolenko M, Aitken D, Hallahan T, Macri J, Buchanan PD.

Prenat Diagn. 2003 May;23(5):385-8.

PMID:
12749035
4.

Frequency of Down's syndrome and neural-tube defects in the same family.

Barkai G, Arbuzova S, Berkenstadt M, Heifetz S, Cuckle H.

Lancet. 2003 Apr 19;361(9366):1331-5.

PMID:
12711468
5.

Mitochondrial dysfunction and Down's syndrome.

Arbuzova S, Hutchin T, Cuckle H.

Bioessays. 2002 Aug;24(8):681-4. Review.

PMID:
12210526
6.

Familial Down syndrome: evidence supporting cytoplasmic inheritance.

Arbuzova S, Cuckle H, Mueller R, Sehmi I.

Clin Genet. 2001 Dec;60(6):456-62.

PMID:
11846739
7.

Maternally inherited hearing impairment in a family with the mitochondrial DNA A7445G mutation.

Hutchin TP, Lench NJ, Arbuzova S, Markham AF, Mueller RF.

Eur J Hum Genet. 2001 Jan;9(1):56-8.

8.

The genetic legacy of Paleolithic Homo sapiens sapiens in extant Europeans: a Y chromosome perspective.

Semino O, Passarino G, Oefner PJ, Lin AA, Arbuzova S, Beckman LE, De Benedictis G, Francalacci P, Kouvatsi A, Limborska S, Marcikiae M, Mika A, Mika B, Primorac D, Santachiara-Benerecetti AS, Cavalli-Sforza LL, Underhill PA.

Science. 2000 Nov 10;290(5494):1155-9.

9.

Maternal blood superoxide dismutase in Down syndrome.

Cuckle H, Arbuzova S.

Prenat Diagn. 2000 Apr;20(4):354-5. No abstract available.

PMID:
10740214
10.

[The use of oxidant-antioxidant system indices in forming groups at high genetic risk].

Arbuzova SB, Fedotova OO, Malova SA, Krasnov AV.

Tsitol Genet. 1999 Jul-Aug;33(4):77-80. Russian.

PMID:
10563382
11.

[The biochemical marker dynamics of the maternal serum in different chromosomal disorders of the fetus].

Arbuzova SB, Nikolenko MI, Khlevnaia LA, Fedotova OO, Solov'eva VD, Malova SA, Krasnov AV.

Tsitol Genet. 1998 Sep-Oct;32(5):75-9. Russian.

PMID:
9879118
12.

[The prenatal diagnosis of Down's syndrome based on the biochemical screening of maternal serum markers].

Arbuzova SB, Nikolenko MI, Khlevnaia LA, Fedotova OO, Solov'eva VD, Malova SA.

Tsitol Genet. 1998 Jan-Feb;32(1):66-71. Russian.

PMID:
9695254
13.

Genetic services in the Ukraine.

Arbuzova S.

Eur J Hum Genet. 1997;5 Suppl 2:183-7. No abstract available.

PMID:
9450221
14.

[The age-dependent incidence of Down's syndrome and the free-radical theory].

Arbuzova SB.

Tsitol Genet. 1996 Sep-Oct;30(5):27-35. Russian.

PMID:
9026987
15.

[Free radicals in the origin and clinical manifestation of Down's syndrome].

Arbuzova SB.

Tsitol Genet. 1996 Mar-Apr;30(2):25-34. Russian.

PMID:
9281201
16.

[The formation of risk groups and the performance of invasive prenatal diagnosis].

Arbuzova SB, Khlevnaia LA, Kaznacheeva EB, Nikolenko MI.

Tsitol Genet. 1995 Sep-Oct;29(5):76-81. Russian.

PMID:
8721851
17.
18.

[The role of mitochondrial DNA in the origin of regular trisomy 21].

Arbuzova SB.

Tsitol Genet. 1995 May-Jun;29(3):77-80. Review. Russian.

PMID:
7676512
19.

[Individual variability in the level of spontaneous sister chromatid exchanges].

Arbuzova SB.

Tsitol Genet. 1988 Mar-Apr;22(2):57-62. Russian.

PMID:
3413821
20.

[Dystrophic dysplasia in siblings].

Arbuzova SB, Zukin VD.

Pediatriia. 1984 Dec;(12):65-6. Russian. No abstract available.

PMID:
6335240
21.

[Trisomy syndrome of the 9th chromosome in a 3-month-old infant].

Dorofeeva GD, Arbuzova SB, Manoń≠lenko ON, Zukin VD.

Pediatriia. 1984 Nov;(11):60-1. Russian. No abstract available.

PMID:
6527918

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