147 related articles for article (PubMed ID: 11603568)
21. A single base substitution in the coding region for neurophysin II associated with familial central diabetes insipidus.
Ito M; Mori Y; Oiso Y; Saito H
J Clin Invest; 1991 Feb; 87(2):725-8. PubMed ID: 1840604
[TBL] [Abstract][Full Text] [Related]
22. Two novel mutations in the coding region for neurophysin-II associated with familial central diabetes insipidus.
Nagasaki H; Ito M; Yuasa H; Saito H; Fukase M; Hamada K; Ishikawa E; Katakami H; Oiso Y
J Clin Endocrinol Metab; 1995 Apr; 80(4):1352-6. PubMed ID: 7714110
[TBL] [Abstract][Full Text] [Related]
23. Familial neurohypophyseal diabetes insipidus associated with a signal peptide mutation.
McLeod JF; Kovács L; Gaskill MB; Rittig S; Bradley GS; Robertson GL
J Clin Endocrinol Metab; 1993 Sep; 77(3):599A-599G. PubMed ID: 8370682
[TBL] [Abstract][Full Text] [Related]
24. A new missense mutation of the vasopressin-neurophysin II gene in a family with neurohypophyseal diabetes insipidus.
Wolf MT; Dötsch J; Metzler M; Holder M; Repp R; Rascher W
Horm Res; 2003; 60(3):143-7. PubMed ID: 12931042
[TBL] [Abstract][Full Text] [Related]
25. Normal MR appearances of the posterior pituitary in central diabetes insipidus associated with septo-optic dysplasia.
Abernethy LJ; Qunibi MA; Smith CS
Pediatr Radiol; 1997 Jan; 27(1):45-7. PubMed ID: 8995167
[TBL] [Abstract][Full Text] [Related]
26. Molecular analysis in familial neurohypophyseal diabetes insipidus: early diagnosis of an asymptomatic carrier.
Calvo B; Bilbao JR; Rodríguez A; Rodríguez-Arnao MD; Castaño L
J Clin Endocrinol Metab; 1999 Sep; 84(9):3351-4. PubMed ID: 10487710
[TBL] [Abstract][Full Text] [Related]
27. Glu-47, which forms a salt bridge between neurophysin-II and arginine vasopressin, is deleted in patients with familial central diabetes insipidus.
Yuasa H; Ito M; Nagasaki H; Oiso Y; Miyamoto S; Sasaki N; Saito H
J Clin Endocrinol Metab; 1993 Sep; 77(3):600-4. PubMed ID: 8103767
[TBL] [Abstract][Full Text] [Related]
28. Familial neurohypophyseal diabetes insipidus associated with a novel mutation in the vasopressin-neurophysin II gene.
Fujii H; Iida S; Moriwaki K
Int J Mol Med; 2000 Mar; 5(3):229-34. PubMed ID: 10677561
[TBL] [Abstract][Full Text] [Related]
29. Early-Onset Central Diabetes Insipidus due to Compound Heterozygosity for AVP Mutations.
Bourdet K; Vallette S; Deladoëy J; Van Vliet G
Horm Res Paediatr; 2016; 85(4):283-7. PubMed ID: 26565711
[TBL] [Abstract][Full Text] [Related]
30. Dilatative uropathy as a manifestation of neurohypophyseal diabetes insipidus due to a novel mutation in the arginine vasopressin-neurophysin-II gene.
Lindenthal V; Mainberger A; Morris-Rosendahl DJ; Löning L; Mayer W; Müller HL
Klin Padiatr; 2013 Dec; 225(7):407-12. PubMed ID: 24158882
[TBL] [Abstract][Full Text] [Related]
31. A novel heterozygous missense mutation in the vasopressin moiety is identified in a Japanese person with neurohypophyseal diabetes insipidus.
Kobayashi H; Fujisawa I; Ikeda K; Son C; Iwakura T; Yoshimoto A; Kasahara M; Ishihara T; Ogawa Y
J Endocrinol Invest; 2006 Mar; 29(3):252-6. PubMed ID: 16682840
[TBL] [Abstract][Full Text] [Related]
32. Familial central diabetes insipidus detected by nocturnal enuresis.
Kanemitsu N; Kawauchi A; Nishida M; Tanaka Y; Mizutani Y; Shirahama S; Miki T
Pediatr Nephrol; 2002 Dec; 17(12):1063-5. PubMed ID: 12478359
[TBL] [Abstract][Full Text] [Related]
33. [Identification of a new mutation (CysII6Gly) in a family with neurogenic diabetes insipidus].
van den Akker EL; de Groot MR; Abbes AP; Bruggeman EJ; Franken AA; Engel H
Ned Tijdschr Geneeskd; 2000 May; 144(20):941-5. PubMed ID: 10827849
[TBL] [Abstract][Full Text] [Related]
34. A missense mutation encoding cys(67) --> gly in neurophysin ii is associated with early onset autosomal dominant neurohypophyseal diabetes insipidus.
DiMeglio LA; Gagliardi PC; Browning JE; Quigley CA; Repaske DR
Mol Genet Metab; 2001 Jan; 72(1):39-44. PubMed ID: 11161827
[TBL] [Abstract][Full Text] [Related]
35. Persistent high MR signal of the posterior pituitary gland in central diabetes insipidus.
Maghnie M; Genovese E; Bernasconi S; Binda S; Aricò M
AJNR Am J Neuroradiol; 1997 Oct; 18(9):1749-52. PubMed ID: 9367327
[TBL] [Abstract][Full Text] [Related]
36. Effects of aging on vasopressin production in a kindred with autosomal dominant neurohypophyseal diabetes insipidus due to the DeltaE47 neurophysin mutation.
Mahoney CP; Weinberger E; Bryant C; Ito M; Jameson JL; Ito M
J Clin Endocrinol Metab; 2002 Feb; 87(2):870-6. PubMed ID: 11836335
[TBL] [Abstract][Full Text] [Related]
37. [Recent progress in the diagnosis and treatment of diabetes insipidus].
Kawakami S; Honda K; Ishikawa S; Saito T
Nihon Rinsho; 1993 Oct; 51(10):2737-41. PubMed ID: 8254949
[TBL] [Abstract][Full Text] [Related]
38. Mutation of Glu78 of the AVP-NPII gene impairs neurophysin as a carrier protein for arginine vasopressin in a family with neurohypophyseal diabetes insipidus.
Lee YW; Lee KW; Ryu JW; Mok JO; Ki CS; Park HK; Kim YJ; Kim SJ; Byun DW; Suh KI; Yoo MH; Shin HB; Lee YK; Kim CH
Ann Clin Lab Sci; 2008; 38(1):12-4. PubMed ID: 18316776
[TBL] [Abstract][Full Text] [Related]
39. Identification of 13 new mutations in the vasopressin-neurophysin II gene in 17 kindreds with familial autosomal dominant neurohypophyseal diabetes insipidus.
Rittig S; Robertson GL; Siggaard C; Kovács L; Gregersen N; Nyborg J; Pedersen EB
Am J Hum Genet; 1996 Jan; 58(1):107-17. PubMed ID: 8554046
[TBL] [Abstract][Full Text] [Related]
40. A novel mutation (R97C) in the neurophysin moiety of prepro-vasopressin-neurophysin II associated with autosomal-dominant neurohypophyseal diabetes insipidus.
Rutishauser J; Kopp P; Gaskill MB; Kotlar TJ; Robertson GL
Mol Genet Metab; 1999 May; 67(1):89-92. PubMed ID: 10329029
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
