• 169 Citations
  • 9 h-Index
1981 …2008

Research output per year

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Research Output

  • 169 Citations
  • 9 h-Index
  • 32 Article
  • 3 Letter
  • 2 Review article
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Article
2007

Izodicentrikus Y-kromoszómához társuló kevert gonáddiszgenezis

Translated title of the contribution: Mixed gonadal dysgenesis associated with an isodicentric Y chromosomeSágodi, L., Sólyom, E., Tóth, A., Kékesi, A., P. Tardy, E., Borbás, É., Rétfalvi, T., Kiss, Á. & Korcsmáros, A., Aug 19 2007, In : Orvosi hetilap. 148, 33, p. 1567-1571 5 p.

Research output: Contribution to journalArticle

9 Citations (Scopus)

Segregation of chromosomes in spermatozoa of four Hungarian translocation carriers

Kékesi, A., Erdei, E., Török, M., Drávucz, S. & Tóth, A., Jul 2007, In : Fertility and Sterility. 88, 1, p. 212.e5-212.e11

Research output: Contribution to journalArticle

13 Citations (Scopus)
2006

Spermiumok aneuploidiájának vizsgálata fluoreszcens in situ hibridizációval kóros spermalelettel rendelkezo férfiaknál

Translated title of the contribution: Investigation of aneuploidy frequency in spermatozoa of males with abnormal semen parameters by fluorescence in situ hybridization (FISH)Kékesi, A., Erdei, E., Dévai, I. & Tóth, A., Aug 9 2006, In : Magyar Noorvosok Lapja. 69, 4, p. 309-316 8 p.

Research output: Contribution to journalArticle

2005

Y;3 transzlokációt hordozó beteg spermiumainak szegregációs analízise fluoreszcens in szitu hibridizációval

Translated title of the contribution: Sperm analysis in an infertile male with a Y-3 translocation, using fluorescent in situ hybridizationKékesi, A., Erdei, E. & Tóth, A., Jun 15 2005, In : Magyar Noorvosok Lapja. 68, 3, p. 173-177 5 p.

Research output: Contribution to journalArticle

2003

A meddo férfiak spermiumainak citogenetikai vizsgálata elso hazai tapasztalatok

Translated title of the contribution: Our first experiences with cytogenetic investigations of sperms at infertile malesTóth, A., Tardy, E. P., Kékesi, A., Drávucz, S., Murányi, Z., Vajda, M., Dévai, I., Cseh, I. & Erdei, E., Jan 1 2003, In : Magyar Noorvosok Lapja. 66, 3, p. 143-147 5 p.

Research output: Contribution to journalArticle

2 Citations (Scopus)
2001

AZFc deletion detected in a newborn with prenatally diagnosed Yq deletion

Toth, A., Tardy, E. P., Gombos, S., Hajdu, K., Batorfi, J. & Krausz, C., May 20 2001, In : Prenatal Diagnosis. 21, 4, p. 253-255 3 p.

Research output: Contribution to journalArticle

6 Citations (Scopus)

Fluorescence in situ hybridization of chorionic interphase cells for prenatal screening of Down syndrome

Tóth, A., Tardy, E. P., Hajdu, K., Bátorfi, J., Doszpod, J., Egyed, J. & Gáti, I., Jan 2001, In : European Journal of Obstetrics Gynecology and Reproductive Biology. 94, 1, p. 46-50 5 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)

Gyors diagnosztikai módszer a Down-szindróma újszülöttkori kimutatására.

Translated title of the contribution: Rapid diagnostic method for detecting Down syndrome in newbornsTardy, E. P. & Tóth, A., Apr 29 2001, In : Orvosi hetilap. 142, 17, p. 895-897 3 p.

Research output: Contribution to journalArticle

2000
1997
9 Citations (Scopus)
1996

A fluoreszcens in situ hibridizáció alkalmazása a praenatalis diagnosztikában. Elsö tapasztalatok.

Translated title of the contribution: Fluorescence in situ hybridization in prenatal diagnosis. First experiencesTardy, E., Tóth, A., Hajdu, K., Gombos, S. & László, J., Mar 10 1996, In : Orvosi hetilap. 137, 10, p. 523-526 4 p.

Research output: Contribution to journalArticle

2 Citations (Scopus)

A VIII. faktor génjének molekuláris biológiai vizsgálata haemophilia A megbetegedésben.

Translated title of the contribution: Molecular biologic study and the factor VIII gene in hemophilia ABock, I., Melegh, B., Nagy, A., Losonczy, H., Csete, B., Schröder, W., Kardos, M., István, L., Jager, R., Tóth, A. M., Tóth, A., Falko, H. & Mózsik, G., Nov 17 1996, In : Orvosi hetilap. 137, 46, p. 2573-2575 3 p.

Research output: Contribution to journalArticle

1992

Tetraploidy in human placenta. A dilemma in molar and non-molar pregnancies

Toth, A., Arato, G., Szepesi, J., Hajdu, K., Szigetvari, I. & Laszlo, J., Jan 1 1992, In : Gynecologic and Obstetric Investigation. 33, 3, p. 153-156 4 p.

Research output: Contribution to journalArticle

4 Citations (Scopus)
1991

Prenatal cytogenetic study of translocation carriers.

Tóth, A., Rajczy, K., Hajdu, K., Intödy, Z. S. & László, J., 1991, In : Acta medica Hungarica. 48, 3-4, p. 151-156 6 p.

Research output: Contribution to journalArticle

Transabdominalis chorion-aspiráció a terhesség második trimesterében.

Translated title of the contribution: Transabdominal chorion aspiration in the second pregnancy trimesterHajdu, K., Intödy, Z., Tóth, A., Rajczy, K. & László, J., Aug 11 1991, In : Orvosi hetilap. 132, 32, p. 1757-1760 4 p.

Research output: Contribution to journalArticle

1990

Az Edwards-syndroma fetális diagnosztikája.

Translated title of the contribution: Fetal diagnosis of Edwards syndromeTóth, A., Hajdu, K., Intödy, Z., Rajczy, K. & László, J., Oct 28 1990, In : Orvosi hetilap. 131, 43, p. 2355-2356, 2359

Research output: Contribution to journalArticle

1988

PARTIELLE MOLE MIT LUNGENMETASTASEN UND MULTIPLEN MISSBILDUNGEN DES FETEN

Translated title of the contribution: Partial hydatidiform mole with mutiple malformations and lung metastasesSzepesi, J., Szigetvari, I., Toth, A., Hajdu, K. & Laszlo, J., Jan 1 1988, In : Zentralblatt fur Gynakologie. 110, 4, p. 246-249 4 p.

Research output: Contribution to journalArticle

4 Citations (Scopus)
1987

Direct chromosomal preparation for studying hydatidiform moles

Tóth, A., Szepesi, J., Szigetvari, I. & László, J., Jan 1 1987, In : Placenta. 8, 6, p. 587-590 4 p.

Research output: Contribution to journalArticle

8 Citations (Scopus)

Endometriosis and streak gonad syndrome

Bösze, P., Gaál, M., Tóth, A. & László, J., Apr 1 1987, In : Archives of Gynecology. 240, 4, p. 253-254 2 p.

Research output: Contribution to journalArticle

10 Citations (Scopus)
1985

A familiárisan elöforduló 46,XX csíkgonád szindróma (Tiszta gonád diszgenesis).

Translated title of the contribution: Familial streak gonad syndrome with 46,XX karyotype (pure gonadal dysgenesis)Tóth, A., Gaál, M., Bösze, P., Komora, V. & László, J., Mar 3 1985, In : Orvosi hetilap. 126, 9, p. 527-529 3 p.

Research output: Contribution to journalArticle

The androgen insensitivity

Bosze, P., Blasko-Turi, Z. & Toth, A., Jan 1 1985, In : Orvoskepzes. 60, 6, p. 449-457 9 p.

Research output: Contribution to journalArticle

1984

46, X, i(Xq)/45, X mosaicism with gonadal dysgenesis associated with 21p‐

Gaál, M., Tóth, A., Bösze, P. & László, J., Jan 1984, In : Clinical Genetics. 25, 1, p. 79-83 5 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)

A case of 44,X streak gonad syndrome combined with familial balanced 13/14 translocation.

László, J., Bösze, P., Gaál, M. & Tóth, A., Dec 1 1984, In : Acta medica Hungarica. 41, 4, p. 223-227 5 p.

Research output: Contribution to journalArticle

5 Citations (Scopus)

Aspiration of chorionic villus material: A new possibility in fetal diagnostics

Intody, Z., Gaal, M., Toth, A. & Laszlo, J., Jan 1 1984, In : Magyar Noorvosok Lapja. 47, 3, p. 233-237 5 p.

Research output: Contribution to journalArticle

Chromosome abnormalities in 118 couples with recurrent spontaneous abortions

Tóth, A., Gaál, M., Bösze, P. & László, J., Jan 1 1984, In : Gynecologic and Obstetric Investigation. 18, 2, p. 72-77 6 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)

Familial pericentric inversion of the Y chromosome

Toth, A., Gaal, M. & Laszlo, J., Jan 1 1984, In : Annales de Genetique. 27, 1, p. 60-61 2 p.

Research output: Contribution to journalArticle

11 Citations (Scopus)

Gonád dysgenesissel szövödött 21p- chromosoma rendellenesség.

Translated title of the contribution: 21p- chromosome abnormality associated with gonadal dysgenesisGaál, M., Tóth, A., Bösze, P. & László, J., Jul 8 1984, In : Orvosi hetilap. 125, 28, p. 1695-1697 3 p.

Research output: Contribution to journalArticle

1983

Perrault's syndrome in two sisters

Bosze, P., Skripeczky, K., Gaal, M., Tóth, A. & László, J., Dec 1 1983, In : American journal of medical genetics. 16, 2, p. 237-221 17 p.

Research output: Contribution to journalArticle

11 Citations (Scopus)
1982

A recesszíven öröklödö hydrocephalus (Prenatális diagnosztikai és kezelési meggondolások).

Translated title of the contribution: Recessive-inherited hydrocephalus (prenatal diagnostic and therapeutic considerations)Bösze, P., Czeizel, E., Kiss, P., Lászlo, J., Papp, Z., Sebök, J., Tóth, A. & Tóth, Z., Mar 21 1982, In : Orvosi hetilap. 123, 12, p. 723-729 7 p.

Research output: Contribution to journalArticle

2 Citations (Scopus)

Pericentric inversion of chromosome 1 in an azoospermic man

Toth, A., Gaal, M., Sara, G. & Laszlo, J., Jan 1 1982, In : Journal of medical genetics. 19, 4, p. 303-305 3 p.

Research output: Contribution to journalArticle

7 Citations (Scopus)

Trisomy 20 mosaicism in amniotic fluid cells

Bösze, P., László, J. & Tóth, A., Jan 1 1982, In : Prenatal Diagnosis. 2, 3, p. 225-227 3 p.

Research output: Contribution to journalArticle

7 Citations (Scopus)
1981

Az 1-es kromoszóma férfi meddöséggel járó öröklödö pericentrikus inverziója.

Translated title of the contribution: Inherited pericentric inversion of the chromosome 1 associated with male infertilityTóth, A., Gaál, M., Sára, G. & László, J., Sep 27 1981, In : Orvosi hetilap. 122, 39, p. 2423-2425 3 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)