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Results: 1 to 20 of 113

1.

Clinical Case Seminar. Peculiar prolactinomas in patients with pituitary developmental gene mutations: from an adult endocrinologist perspective.

Doknic M, Pekic S, Civcic M, Popovic V.

Hormones (Athens). 2012 Apr-Jun;11(2):189-98.

PMID:
22801565
[PubMed - indexed for MEDLINE]
Free Article
2.

Case seminar: a young female with acute hyponatremia and a sellar mass.

Pekic S, Doknic M, Miljic D, Saveanu A, Reynaud R, Barlier A, Brue T, Popovic V.

Endocrine. 2011 Dec;40(3):325-31. doi: 10.1007/s12020-011-9516-8. Epub 2011 Aug 24.

PMID:
21863341
[PubMed - indexed for MEDLINE]
3.

PROP1 gene analysis in Portuguese patients with combined pituitary hormone deficiency.

Lemos MC, Gomes L, Bastos M, Leite V, Limbert E, Carvalho D, Bacelar C, Monteiro M, Fonseca F, Agapito A, Castro JJ, Regateiro FJ, Carvalheiro M.

Clin Endocrinol (Oxf). 2006 Oct;65(4):479-85.

PMID:
16984240
[PubMed - indexed for MEDLINE]
4.

Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).

Turton JP, Mehta A, Raza J, Woods KS, Tiulpakov A, Cassar J, Chong K, Thomas PQ, Eunice M, Ammini AC, Bouloux PM, Starzyk J, Hindmarsh PC, Dattani MT.

Clin Endocrinol (Oxf). 2005 Jul;63(1):10-8.

PMID:
15963055
[PubMed - indexed for MEDLINE]
5.

Novel fibroblast growth factor receptor 1 mutations in patients with congenital hypogonadotropic hypogonadism with and without anosmia.

Trarbach EB, Costa EM, Versiani B, de Castro M, Baptista MT, Garmes HM, de Mendonca BB, Latronico AC.

J Clin Endocrinol Metab. 2006 Oct;91(10):4006-12. Epub 2006 Aug 1. Erratum in: J Clin Endocrinol Metab. 2008 May;93(5):2013.

PMID:
16882753
[PubMed - indexed for MEDLINE]
6.

[Homeoproteins and pituitary adenoma].

Barlier A, Pellegrini-Bouiller I, Gunz G, Jaquet P, Enjalbert A.

Ann Endocrinol (Paris). 1997;58(1):3-10. Review. French.

PMID:
9207961
[PubMed - indexed for MEDLINE]
7.

[Genetic background of inherited multiple pituitary hormone deficiency. Mutations of PROP1 gene in Hungary].

Halász Z.

Orv Hetil. 2011 Feb 6;152(6):221-32. doi: 10.1556/OH.2011.29032. Hungarian.

PMID:
21278027
[PubMed - indexed for MEDLINE]
Free Article
8.

Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutation.

Riepe FG, Partsch CJ, Blankenstein O, Mönig H, Pfäffle RW, Sippell WG.

J Clin Endocrinol Metab. 2001 Sep;86(9):4353-7.

PMID:
11549674
[PubMed - indexed for MEDLINE]
9.

Hypopituitarism oddities: congenital causes.

Kelberman D, Dattani MT.

Horm Res. 2007;68 Suppl 5:138-44. doi: 10.1159/000110610. Epub 2007 Dec 10. Review.

PMID:
18174732
[PubMed - indexed for MEDLINE]
10.

A mutation in the fibroblast growth factor receptor 1 gene causes fully penetrant normosmic isolated hypogonadotropic hypogonadism.

Xu N, Qin Y, Reindollar RH, Tho SP, McDonough PG, Layman LC.

J Clin Endocrinol Metab. 2007 Mar;92(3):1155-8. Epub 2007 Jan 2.

PMID:
17200176
[PubMed - indexed for MEDLINE]
11.

Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.

Pitteloud N, Meysing A, Quinton R, Acierno JS Jr, Dwyer AA, Plummer L, Fliers E, Boepple P, Hayes F, Seminara S, Hughes VA, Ma J, Bouloux P, Mohammadi M, Crowley WF Jr.

Mol Cell Endocrinol. 2006 Jul 25;254-255:60-9. Epub 2006 Jun 9.

PMID:
16764984
[PubMed - indexed for MEDLINE]
12.

Complex genetics in idiopathic hypogonadotropic hypogonadism.

Pitteloud N, Durrani S, Raivio T, Sykiotis GP.

Front Horm Res. 2010;39:142-53. doi: 10.1159/000312700. Epub 2010 Apr 8. Review.

PMID:
20389092
[PubMed - indexed for MEDLINE]
13.

Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene.

Pernasetti F, Toledo SP, Vasilyev VV, Hayashida CY, Cogan JD, Ferrari C, Lourenço DM Jr, Mellon PL.

J Clin Endocrinol Metab. 2000 Jan;85(1):390-7.

PMID:
10634415
[PubMed - indexed for MEDLINE]
14.

High prevalence of PROP1 gene mutations in Hungarian patients with childhood-onset combined anterior pituitary hormone deficiency.

Halász Z, Toke J, Patócs A, Bertalan R, Tömböl Z, Sallai A, Hosszú E, Muzsnai A, Kovács L, Sólyom J, Fekete G, Rácz K.

Endocrine. 2006 Dec;30(3):255-60.

PMID:
17526936
[PubMed - indexed for MEDLINE]
15.

A critical functional missense mutation (H173R) in the bovine PROP1 gene significantly affects growth traits in cattle.

Pan C, Wu C, Jia W, Xu Y, Lei C, Hu S, Lan X, Chen H.

Gene. 2013 Dec 1;531(2):398-402. doi: 10.1016/j.gene.2013.09.002. Epub 2013 Sep 10.

PMID:
24029076
[PubMed - indexed for MEDLINE]
16.

Submicroscopic deletion involving the fibroblast growth factor receptor 1 gene in a patient with combined pituitary hormone deficiency.

Fukami M, Iso M, Sato N, Igarashi M, Seo M, Kazukawa I, Kinoshita E, Dateki S, Ogata T.

Endocr J. 2013;60(8):1013-20. Epub 2013 May 9.

PMID:
23657145
[PubMed - indexed for MEDLINE]
Free Article
17.

Increased abnormal pituitary findings on magnetic resonance in patients with male idiopathic hypogonadotrophic hypogonadism.

Bolu SE, Tasar M, Uçkaya G, Gönül E, Deniz F, Ozdemir IC.

J Endocrinol Invest. 2004 Dec;27(11):1029-33.

PMID:
15754734
[PubMed - indexed for MEDLINE]
18.

Pituitary prolactin-secreting tumor formation: recent developments.

Xu RK, Wu XM, Di AK, Xu JN, Pang CS, Pang SF.

Biol Signals Recept. 2000 Jan-Feb;9(1):1-20. Review.

PMID:
10686432
[PubMed - indexed for MEDLINE]
19.

Central hypocortisolism as part of combined pituitary hormone deficiency due to mutations of PROP-1 gene.

Asteria C, Oliveira JH, Abucham J, Beck-Peccoz P.

Eur J Endocrinol. 2000 Sep;143(3):347-52.

PMID:
11022176
[PubMed - indexed for MEDLINE]
Free Article
20.

MR imaging of the pituitary gland in children and young adults with congenital combined pituitary hormone deficiency associated with PROP1 mutations.

Fofanova O, Takamura N, Kinoshita E, Vorontsov A, Vladimirova V, Dedov I, Peterkova V, Yamashita S.

AJR Am J Roentgenol. 2000 Feb;174(2):555-9.

PMID:
10658742
[PubMed - indexed for MEDLINE]

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