Lorenzen F - Search Results

1

"Acquired" adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorders as congenital adrenal hyperplasia.

New MI, Lorenzen F, Pang S, Gunczler P, Dupont B, Levine LS. New MI, et al. Among authors: lorenzen f. J Clin Endocrinol Metab. 1979 Feb;48(2):356-9. doi: 10.1210/jcem-48-2-356. J Clin Endocrinol Metab. 1979. PMID: 218988

2

Hormonal phenotype and HLA-genotype in families of patients with congenital adrenal hyperplasia (21-hydroxylase deficiency).

Lorenzen F, Pang S, New MI, Dupont B, Pollack M, Chow DM, Levine LS. Lorenzen F, et al. Pediatr Res. 1979 Dec;13(12):1356-60. doi: 10.1203/00006450-197912000-00011. Pediatr Res. 1979. PMID: 230448

3

Studies of the C-21 and C-19 steroids and HLA genotyping in siblings and parents of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Lorenzen F, Pang S, New M, Pollack M, Oberfield S, Dupont B, Chow D, Schneider B, Levine L. Lorenzen F, et al. J Clin Endocrinol Metab. 1980 Mar;50(3):572-7. doi: 10.1210/jcem-50-3-572. J Clin Endocrinol Metab. 1980. PMID: 6244326 No abstract available.

4

Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasia.

Pang S, Levine LS, Lorenzen F, Chow D, Pollack M, Dupont B, Genel M, New MI. Pang S, et al. Among authors: lorenzen f. J Clin Endocrinol Metab. 1980 Mar;50(3):586-9. doi: 10.1210/jcem-50-3-586. J Clin Endocrinol Metab. 1980. PMID: 6244328

5

Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency.

Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield SE, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI. Levine LS, et al. Among authors: lorenzen f. J Clin Endocrinol Metab. 1981 Dec;53(6):1193-8. doi: 10.1210/jcem-53-6-1193. J Clin Endocrinol Metab. 1981. PMID: 6271801

6

Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia.

Kohn B, Levine LS, Pollack MS, Pang S, Lorenzen F, Levy D, Lerner AJ, Rondanini GF, Dupont B, New MI. Kohn B, et al. Among authors: lorenzen f. J Clin Endocrinol Metab. 1982 Nov;55(5):817-27. doi: 10.1210/jcem-55-5-817. J Clin Endocrinol Metab. 1982. PMID: 6288753

7

Genotyping steroid 21-hydroxylase deficiency: hormonal reference data.

New MI, Lorenzen F, Lerner AJ, Kohn B, Oberfield SE, Pollack MS, Dupont B, Stoner E, Levy DJ, Pang S, Levine LS. New MI, et al. Among authors: lorenzen f. J Clin Endocrinol Metab. 1983 Aug;57(2):320-6. doi: 10.1210/jcem-57-2-320. J Clin Endocrinol Metab. 1983. PMID: 6306039

8

Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.

Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield S, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI. Levine LS, et al. Among authors: lorenzen f. J Clin Endocrinol Metab. 1980 Dec;51(6):1316-24. doi: 10.1210/jcem-51-6-1316. J Clin Endocrinol Metab. 1980. PMID: 6449518

9

Detection of heterozygote of 21-hydroxylase deficiency.

Levine LS, Pang S, Dupont B, Pollack M, Lorenzen F, New MI. Levine LS, et al. Among authors: lorenzen f. Lancet. 1980 Mar 15;1(8168 Pt 1):603-4. doi: 10.1016/s0140-6736(80)91097-1. Lancet. 1980. PMID: 6102330 No abstract available.

10

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. Laron Z, et al. Among authors: lorenzen f. Hum Immunol. 1980 Jul;1(1):55-66. doi: 10.1016/0198-8859(80)90009-9. Hum Immunol. 1980. PMID: 6266983 No abstract available.

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