Your browser version may not work well with NCBI's Web applications. More information here...

Recent Activity

Items 1 - 20 of 100
of 5Next
1:

Clinical and inheritance profiles of Kallmann syndrome in Jordan.

Abujbara MA, Hamamy HA, Jarrah NS, Shegem NS, Ajlouni KM.

Reprod Health. 2004 Oct 24;1(1):5.

PMID: 15500697 [PubMed - as supplied by publisher]

2:

The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics.

Oliveira LM, Seminara SB, Beranova M, Hayes FJ, Valkenburgh SB, Schipani E, Costa EM, Latronico AC, Crowley WF Jr, Vallejo M.

J Clin Endocrinol Metab. 2001 Apr;86(4):1532-8.

PMID: 11297579 [PubMed - indexed for MEDLINE]

3:

Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization.

Quinton R, Duke VM, Robertson A, Kirk JM, Matfin G, de Zoysa PA, Azcona C, MacColl GS, Jacobs HS, Conway GS, Besser M, Stanhope RG, Bouloux PM.

Clin Endocrinol (Oxf). 2001 Aug;55(2):163-74.

PMID: 11531922 [PubMed - indexed for MEDLINE]

4:

Clinical and inheritance profiles of hyperekplexia in Jordan.

Masri AT, Hamamy HA.

J Child Neurol. 2007 Jul;22(7):895-900.

PMID: 17715287 [PubMed - indexed for MEDLINE]

5:

The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human.

Waldstreicher J, Seminara SB, Jameson JL, Geyer A, Nachtigall LB, Boepple PA, Holmes LB, Crowley WF Jr.

J Clin Endocrinol Metab. 1996 Dec;81(12):4388-95.

PMID: 8954047 [PubMed - indexed for MEDLINE]

6:

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]

7:

[GnRH deficiency: new insights from genetics]

Kottler ML, Hamel A, Malville E, Richard N.

J Soc Biol. 2004;198(1):80-7. Review. French.

PMID: 15146960 [PubMed - indexed for MEDLINE]

8:

Familial patterns of thoracic aortic aneurysms.

Coady MA, Davies RR, Roberts M, Goldstein LJ, Rogalski MJ, Rizzo JA, Hammond GL, Kopf GS, Elefteriades JA.

Arch Surg. 1999 Apr;134(4):361-7.

PMID: 10199307 [PubMed - indexed for MEDLINE]

9:

Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome.

Hardelin JP, Levilliers J, Blanchard S, Carel JC, Leutenegger M, Pinard-Bertelletto JP, Bouloux P, Petit C.

Hum Mol Genet. 1993 Apr;2(4):373-7.

PMID: 8504298 [PubMed - indexed for MEDLINE]

10:

Molecular analysis of KAL-1, GnRH-R, NELF and EBF2 genes in a series of Kallmann syndrome and normosmic hypogonadotropic hypogonadism patients.

Trarbach EB, Baptista MT, Garmes HM, Hackel C.

J Endocrinol. 2005 Dec;187(3):361-8.

PMID: 16423815 [PubMed - indexed for MEDLINE]

11:

Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.

Sato N, Katsumata N, Kagami M, Hasegawa T, Hori N, Kawakita S, Minowada S, Shimotsuka A, Shishiba Y, Yokozawa M, Yasuda T, Nagasaki K, Hasegawa D, Hasegawa Y, Tachibana K, Naiki Y, Horikawa R, Tanaka T, Ogata T.

J Clin Endocrinol Metab. 2004 Mar;89(3):1079-88.

PMID: 15001591 [PubMed - indexed for MEDLINE]

12:

Prophylactic Oophorectomy: Reducing the U.S. Death Rate from Epithelial Ovarian Cancer. A Continuing Debate.

Piver MS.

Oncologist. 1996;1(5):326-330.

PMID: 10388011 [PubMed - as supplied by publisher]

13:

Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism.

Bhagavath B, Podolsky RH, Ozata M, Bolu E, Bick DP, Kulharya A, Sherins RJ, Layman LC.

Fertil Steril. 2006 Mar;85(3):706-13.

PMID: 16500342 [PubMed - indexed for MEDLINE]

14:

The role of prior pubertal development, biochemical markers of testicular maturation, and genetics in elucidating the phenotypic heterogeneity of idiopathic hypogonadotropic hypogonadism.

Pitteloud N, Hayes FJ, Boepple PA, DeCruz S, Seminara SB, MacLaughlin DT, Crowley WF Jr.

J Clin Endocrinol Metab. 2002 Jan;87(1):152-60.

PMID: 11788640 [PubMed - indexed for MEDLINE]

15:

Renal abnormalities in patients with Kallmann syndrome.

Zenteno JC, Méndez JP, Maya-Núñez G, Ulloa-Aguirre A, Kofman-Alfaro S.

BJU Int. 1999 Mar;83(4):383-6.

PMID: 10210557 [PubMed - indexed for MEDLINE]

16:

Clinical evaluation in isolated hypogonadotrophic hypogonadism (Kallmann syndrome).

Dissaneevate P, Warne GL, Zacharin MR.

J Pediatr Endocrinol Metab. 1998 Sep-Oct;11(5):631-8.

PMID: 9829214 [PubMed - indexed for MEDLINE]

17:

Autosomal recessive Alport syndrome: linkage analysis and clinical features in two families.

Torra R, Badenas C, Cofán F, Callis L, Pérez-Oller L, Darnell A.

Nephrol Dial Transplant. 1999 Mar;14(3):627-30.

PMID: 10193810 [PubMed - indexed for MEDLINE]

18:

X chromosome-linked Kallmann syndrome: clinical heterogeneity in three siblings carrying an intragenic deletion of the KAL-1 gene.

Massin N, Pêcheux C, Eloit C, Bensimon JL, Galey J, Kuttenn F, Hardelin JP, Dodé C, Touraine P.

J Clin Endocrinol Metab. 2003 May;88(5):2003-8.

PMID: 12727945 [PubMed - indexed for MEDLINE]

19:

A novel aminoterminal mutation in the KAL-1 gene in a large pedigree with X-linked Kallmann syndrome.

Gu WX, Colquhoun-Kerr JS, Kopp P, Bode HH, Jameson JL.

Mol Genet Metab. 1998 Sep;65(1):59-61.

PMID: 9787096 [PubMed - indexed for MEDLINE]

20:

Renal dysgenesis and KAL1 gene defects in patients with sporadic Kallmann syndrome.

Georgopoulos NA, Koika V, Galli-Tsinopoulou A, Spiliotis BE, Adonakis G, Keramida MK, Sgourou A, Koufogiannis KD, Papachatzopoulou A, Papavassiliou AG, Kourounis G, Vagenakis GA.

Fertil Steril. 2007 Nov;88(5):1311-7. Epub 2007 Jul 2.

PMID: 17603054 [PubMed - indexed for MEDLINE]

Items 1 - 20 of 100
of 5Next