177 related articles for article (PubMed ID: 1682970)
1. Gene probe analysis in an informative family with multiple endocrine neoplasia syndrome type 2A (MEN 2A). Improvement in carrier risk estimation.
Morrison PJ; Hadden DR; Hughes AE; Kennedy L; Russell CJ; Nevin NC
Q J Med; 1991 Jul; 80(291):597-603. PubMed ID: 1682970
[TBL] [Abstract][Full Text] [Related]
2. Clinical screening as compared with DNA analysis in families with multiple endocrine neoplasia type 2A.
Lips CJ; Landsvater RM; Höppener JW; Geerdink RA; Blijham G; van Veen JM; van Gils AP; de Wit MJ; Zewald RA; Berends MJ
N Engl J Med; 1994 Sep; 331(13):828-35. PubMed ID: 7915822
[TBL] [Abstract][Full Text] [Related]
3. [Endocrine polyadenomatosis of 2a type (MEN 2a). Clinical and genetic study of a family].
Guillausseau PJ; Guillausseau C; Calmettes C; Feingold N; Demenais F; Sobol H; Gony J; Hors J; Schaison G; Seret D
Ann Endocrinol (Paris); 1988; 49(1):17-21. PubMed ID: 2900619
[TBL] [Abstract][Full Text] [Related]
4. Characteristics of a family with the MEN-2A syndrome.
Haak HR; Nieuwenhuijzen Kruseman AC
Henry Ford Hosp Med J; 1987; 35(2-3):104-6. PubMed ID: 2891639
[No Abstract] [Full Text] [Related]
5. [A family with type 2a multiple endocrine neoplasms].
Haak HR; Vierhout PA; Vink M; Nieuwenhuyzen Kruseman AC
Ned Tijdschr Geneeskd; 1988 Sep; 132(36):1660-4. PubMed ID: 2902520
[No Abstract] [Full Text] [Related]
6. Early detection of hereditary medullary thyroid cancer with polymorphic DNA probes. Groupe d'Etude des Tumeurs a Calcitonine.
Narod SA; Sobol H; Schuffenecker I; Ezekowitz RA; Lenoir GM
Henry Ford Hosp Med J; 1989; 37(3-4):106-8. PubMed ID: 2576937
[TBL] [Abstract][Full Text] [Related]
7. Multiple endocrine neoplasia type 2A (MEN-2A): natural history, screening, and central registration.
Brouwers-Smalbraak GJ; Vasen HF; Struyvenberg A; Nieuwenhuijzen Kruseman AC; Helsloot MH; Lips CJ
Neth J Med; 1986; 29(4):111-7. PubMed ID: 2872602
[No Abstract] [Full Text] [Related]
8. Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes.
Moley JF; Brother MB; Fong CT; White PS; Baylin SB; Nelkin B; Wells SA; Brodeur GM
Cancer Res; 1992 Feb; 52(4):770-4. PubMed ID: 1346584
[TBL] [Abstract][Full Text] [Related]
9. [Multiple endocrine adenomatosis type II-a: presentation of a stricken family].
García H; Pou J; Moreiro J
Med Clin (Barc); 1987 May; 88(17):689-92. PubMed ID: 2886708
[No Abstract] [Full Text] [Related]
10. Thyroid C-cell hyperplasia and micronodules in close relatives of MEN-2A patients: pitfalls in early diagnosis and reevaluation of criteria for surgery.
Lips CJ; Leo JR; Berends MJ; Minder WH; Blok AP; Geerdink RA; Hackeng WH; Roelofs JM; Vasen HF; Vette JK
Henry Ford Hosp Med J; 1987; 35(2-3):133-8. PubMed ID: 2891645
[No Abstract] [Full Text] [Related]
11. Multiple endocrine neoplasia type 2A: a Northern Ireland and Australian family.
Hadden DR; O'Reilly F; Kennedy L; Russell C
Henry Ford Hosp Med J; 1987; 35(2-3):107-9. PubMed ID: 2891640
[No Abstract] [Full Text] [Related]
12. [Multiple endocrine neoplasm syndrome (MEN-2a) or Sipple syndrome. Report of 2 cases].
Sánchez Román J; Morales Méndez S; Conde García J; Vaquero Ruiz F
Rev Clin Esp; 1983 Jul 15-31; 170(1-2):45-9. PubMed ID: 6138823
[No Abstract] [Full Text] [Related]
13. Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A.
Lairmore TC; Howe JR; Korte JA; Dilley WG; Aine L; Aine E; Wells SA; Donis-Keller H
Genomics; 1991 Jan; 9(1):181-92. PubMed ID: 1672289
[TBL] [Abstract][Full Text] [Related]
14. [Multiple endocrine neoplasm type II-A].
Díaz de Greñu Martínez C; Menéndez Torre EL; Boix Pallarés P; Aller Granda J; Díaz Cadorniga FJ; Rabal Artal A
Med Clin (Barc); 1985 Nov; 85(18):756-8. PubMed ID: 2869204
[No Abstract] [Full Text] [Related]
15. Hereditary medullary thyroid carcinoma: genetic annalysis of three related syndromes. Groupe d'Etude des Tumeurs a Calcitonine.
Sobol H; Narod SA; Schuffenecker I; Amos C; Ezekowitz RA; Lenoir GM
Henry Ford Hosp Med J; 1989; 37(3-4):109-11. PubMed ID: 2576938
[TBL] [Abstract][Full Text] [Related]
16. Multiple endocrine neoplasia type IIb: a description of several patients and review of the literature.
Montgomery TB; Mandelstam P; Tachman ML; Miller RE; Powell DE; Flueck JA; Kotchen TA
J Clin Hypertens; 1987 Mar; 3(1):31-49. PubMed ID: 2883264
[TBL] [Abstract][Full Text] [Related]
17. Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas.
Khosla S; Patel VM; Hay ID; Schaid DJ; Grant CS; van Heerden JA; Thibodeau SN
J Clin Invest; 1991 May; 87(5):1691-9. PubMed ID: 2022740
[TBL] [Abstract][Full Text] [Related]
18. Multiple endocrine neoplasia, type II: a combined surgical and genetic approach to treatment.
Partington MW; Ghent WR; Sears EV; Simpson NE
Can Med Assoc J; 1981 Feb; 124(4):403-10. PubMed ID: 7214269
[TBL] [Abstract][Full Text] [Related]
19. [Familial Sipple's syndrome. Reflections apropos of 4 cases and a survey on 26 members of a family].
Pedinielli L; Argème M
Chirurgie; 1984; 110(4):380-9. PubMed ID: 6149895
[No Abstract] [Full Text] [Related]
20. [Genetic analysis of RET mutations in families with multiple endocrine neoplasia type II in the community of Murcia].
Pomares Gómez FJ; Bernabé Espinosa MJ; Matías-Guiu Guía X; Rodríguez González JM; Soriano Palao J; Sola Pérez J; Carbonell Meseguer P; Parrilla Paricio P; Tébar Massó FJ
Med Clin (Barc); 1999 May; 112(17):646-50. PubMed ID: 10374185
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]