Friedman E - Search Results

1

Studies in a kindred with parathyroid carcinoma.

Streeten EA, Weinstein LS, Norton JA, Mulvihill JJ, White BJ, Friedman E, Jaffe G, Brandi ML, Stewart K, Zimering MB, et al. Streeten EA, et al. Among authors: friedman e. J Clin Endocrinol Metab. 1992 Aug;75(2):362-6. doi: 10.1210/jcem.75.2.1639936. J Clin Endocrinol Metab. 1992. PMID: 1639936

2

Genetic abnormalities in sporadic parathyroid adenomas.

Friedman E, Bale AE, Marx SJ, Norton JA, Arnold A, Tu T, Aurbach GD, Spiegel AM. Friedman E, et al. J Clin Endocrinol Metab. 1990 Aug;71(2):293-7. doi: 10.1210/jcem-71-2-293. J Clin Endocrinol Metab. 1990. PMID: 2199477

3

Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1.

Friedman E, Sakaguchi K, Bale AE, Falchetti A, Streeten E, Zimering MB, Weinstein LS, McBride WO, Nakamura Y, Brandi ML, et al. Friedman E, et al. N Engl J Med. 1989 Jul 27;321(4):213-8. doi: 10.1056/NEJM198907273210402. N Engl J Med. 1989. PMID: 2568586

4

Allelic loss from chromosome 11 in parathyroid tumors.

Friedman E, De Marco L, Gejman PV, Norton JA, Bale AE, Aurbach GD, Spiegel AM, Marx SJ. Friedman E, et al. Cancer Res. 1992 Dec 15;52(24):6804-9. Cancer Res. 1992. PMID: 1360870

5

Activating mutations of the stimulatory G protein in the McCune-Albright syndrome.

Weinstein LS, Shenker A, Gejman PV, Merino MJ, Friedman E, Spiegel AM. Weinstein LS, et al. Among authors: friedman e. N Engl J Med. 1991 Dec 12;325(24):1688-95. doi: 10.1056/NEJM199112123252403. N Engl J Med. 1991. PMID: 1944469 Free article.

6

Allelic loss on chromosome 11 in hereditary and sporadic tumors related to familial multiple endocrine neoplasia type 1.

Bale AE, Norton JA, Wong EL, Fryburg JS, Maton PN, Oldfield EH, Streeten E, Aurbach GD, Brandi ML, Friedman E, et al. Bale AE, et al. Among authors: friedman e. Cancer Res. 1991 Feb 15;51(4):1154-7. Cancer Res. 1991. PMID: 1671755

7

Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis.

Weinstein LS, Gejman PV, Friedman E, Kadowaki T, Collins RM, Gershon ES, Spiegel AM. Weinstein LS, et al. Among authors: friedman e. Proc Natl Acad Sci U S A. 1990 Nov;87(21):8287-90. doi: 10.1073/pnas.87.21.8287. Proc Natl Acad Sci U S A. 1990. PMID: 2122458 Free PMC article.

8

MEN1 gene mutation analysis in Italian patients with multiple endocrine neoplasia type 1.

Morelli A, Falchetti A, Martineti V, Becherini L, Mark M, Friedman E, Brandi ML. Morelli A, et al. Among authors: friedman e. Eur J Endocrinol. 2000 Feb;142(2):131-7. doi: 10.1530/eje.0.1420131. Eur J Endocrinol. 2000. PMID: 10664520

9

Familial isolated hyperparathyroidism: a distinct genetic entity with an increased risk of parathyroid cancer.

Wassif WS, Moniz CF, Friedman E, Wong S, Weber G, Nordenskjöld M, Peters TJ, Larsson C. Wassif WS, et al. Among authors: friedman e. J Clin Endocrinol Metab. 1993 Dec;77(6):1485-9. doi: 10.1210/jcem.77.6.7903311. J Clin Endocrinol Metab. 1993. PMID: 7903311

10

Microsatellite instability in sporadic parathyroid adenoma.

Sarquis M, Friedman E, Boson WL, Gomez RS, Dias AF, De Marco L. Sarquis M, et al. Among authors: friedman e. J Clin Endocrinol Metab. 2000 Jan;85(1):250-2. doi: 10.1210/jcem.85.1.6370. J Clin Endocrinol Metab. 2000. PMID: 10634395

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