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Results: 1 to 20 of 107

1.

Unusual heterozygotes of congenital adrenal hyperplasia due to 21-hydroxylase deficiency confirmed by HLA tissue typing.

Zachmann M, Prader A.

Acta Endocrinol (Copenh). 1979 Nov;92(3):542-6.

PMID:
517053
[PubMed - indexed for MEDLINE]
2.

[Study of the transmission of the 21-hydroxylase deficiency through the hormonal screening and the HLA-typing (author's transl)].

Bartolotta E, Migliori C, Gabrielli A, Oggiano N, Catassi C, Leone L.

Pediatr Med Chir. 1981 Jul-Aug;3(4):287-90. Italian. No abstract available.

PMID:
6283486
[PubMed - indexed for MEDLINE]
3.
4.

Unusual heterozygotes of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Zachmann M, Prader A.

Acta Endocrinol (Copenh). 1978 Mar;87(3):557-65.

PMID:
580145
[PubMed - indexed for MEDLINE]
5.

[Detection of heterozygous carriers of 21-hydroxylase deficiency-HLA typing and endocrinological study (author's transl)].

Saito N, Kuribayashi T, Shimozawa K, Nakagawa S, Tomita M.

Horumon To Rinsho. 1980 Jul;28(7):767-72. Japanese. No abstract available.

PMID:
7460327
[PubMed - indexed for MEDLINE]
6.

Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typing.

Pollack MS, Maurer D, Levine LS, New MI, Pang S, Duchon M, Owens RP, Merkatz IR, Nitowsky BM, Sachs G, Dupont B.

Lancet. 1979 May 26;1(8126):1107-8.

PMID:
86832
[PubMed - indexed for MEDLINE]
7.

Prenatal diagnosis of congenital adrenal hyperplasia.

Marcus ES, Holcombe JH, Tulchinsky D, Rich RR, Riccardi VM.

Am J Med Genet. 1979;4(2):201-4.

PMID:
517576
[PubMed - indexed for MEDLINE]
8.
9.

[Connection between congenital adrenal hyperplasia due to 21-hydroxylase deficiency and the HLA genotype].

Dumić M, Brkljacić L, Krzisnik C, Radica A, Tajić M, Kastelan A.

Lijec Vjesn. 1983 Jul-Aug;105(7-8):290-2. Croatian. No abstract available.

PMID:
6605467
[PubMed - indexed for MEDLINE]
10.

Detection of heterozygotes for congenital adrenal hyperplasia: 21-hydroxylase deficiency-a comparison of HLA typing and 17-OH progesterone response to ACTH infusion.

Mauseth RS, Hansen JA, Smith EK, Giblett ER, Kelley VC.

J Pediatr. 1980 Nov;97(5):749-53.

PMID:
6253614
[PubMed - indexed for MEDLINE]
11.

'Cryptic' form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in the Yugoslav population.

Dumić M, Brkljacić L, Mardesić D, Plavsić V, Lukenda M, Kastelan A.

Acta Endocrinol (Copenh). 1985 Jul;109(3):386-92.

PMID:
2992207
[PubMed - indexed for MEDLINE]
12.

[A genetic and hormonal study of 5 patients with the nonclassical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency].

Velasco FJ, Picó AM, Muñoz C, Mauri M, de la Sen ML.

Med Clin (Barc). 1992 Jun 13;99(3):81-6. Spanish.

PMID:
1321317
[PubMed - indexed for MEDLINE]
13.

[21-hydroxylase deficiency: a case in a newborn revealing a maternal forme tardive].

Simonin G, Palix C, Roulier R, Coignet J.

Ann Pediatr (Paris). 1986 May;33(5):423-7. French. No abstract available.

PMID:
3729253
[PubMed - indexed for MEDLINE]
14.

[Detection of heterozygosity in congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in the general population].

Dumić M, Lukenda M, Plavsić V, Brkljacić L, Jovanović V, Kastelan A.

Lijec Vjesn. 1990 May-Jun;112(5-6):138-41. Croatian.

PMID:
2172673
[PubMed - indexed for MEDLINE]
15.

Sharing of MHC haplotypes among apparently unrelated patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Layrisse Z, White C, Gunczler P, Gafaro Valera L, Arias S, Yunis EJ, Alper CA, Awdeh ZL.

Immunogenetics. 1987;25(2):99-103.

PMID:
3493216
[PubMed - indexed for MEDLINE]
16.

21-Hydroxylase deficiency: HLA genotypes and hormonal phenotypes in the families of 32 Italian patients.

Livieri C, Belvedere M, Martinetti M, Beluffi G, Fiori P, Cogliati CR, Goffredo V, Lorini R, Severi F.

Prog Clin Biol Res. 1985;200:243-55. No abstract available.

PMID:
3001775
[PubMed - indexed for MEDLINE]
17.

[Detection of heterozygotes in the classic type of congenital adrenal hyperplasia due to a 21-hydroxylase defect in our population as based on hormonal studies and HLA typing].

Dumić M, Tajić M, Brkljacić L, Mardesić D, Radica A, Lukenda M, Gjurić G, Jovanović V, Plavsić V, Kastelan A.

Lijec Vjesn. 1984 Nov-Dec;106(11-12):466-70. Croatian. No abstract available.

PMID:
6335215
[PubMed - indexed for MEDLINE]
18.

Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: a new allele at the 21-hydroxylase locus.

Laron Z, Pollack MS, Zamir R, Roitman A, Dickerman Z, Levine LS, Lorenzen F, O'Neill GJ, Pang S, New MI, Dupont B.

Hum Immunol. 1980 Jul;1(1):55-66. No abstract available.

PMID:
6266983
[PubMed - indexed for MEDLINE]
19.

Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their families.

Larizza D, Cuccia M, Martinetti M, Maghnie M, Dondi E, Salvaneschi L, Severi F.

Clin Endocrinol (Oxf). 1994 Jan;40(1):39-45.

PMID:
8306479
[PubMed - indexed for MEDLINE]
20.

Improved test to identify heterozygotes for congenital adrenal hyperplasia without index case examination.

Peter M, Sippell WG, Lorenzen F, Willig RP, Westphal E, Grosse-Wilde H.

Lancet. 1990 Jun 2;335(8701):1296-9.

PMID:
1971375
[PubMed - indexed for MEDLINE]

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