A. M. Spiegel

发表

A familial syndrome of decrease in sensitivity to 1,25-dihydroxyvitamin D.

H. DeLuca, E. Brown, D. Gardner, 1978, The Journal of clinical endocrinology and metabolism.

Resistance to multiple hormones in patients with pseudohypoparathyroidism. Association with deficient activity of guanine nucleotide regulatory protein.

R. Lasker, A. Spiegel, S. Marx, 1983, The American journal of medicine.

Autosomal Dominant Hypocalcemia in Monozygotic Twins Caused by a De Novo Germline Mutation Near the Amino‐Terminus of the Human Calcium Receptor

S. Mora, A. Spiegel, Jianxin Hu, 2004, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

An association between neonatal severe primary hyperparathyroidism and familial hypocalciuric hypercalcemia in three kindreds.

R. Lasker, A. Spiegel, S. Marx, 1982, The New England journal of medicine.

The Hypocalciuric or Benign Variant of Familial Hypercalcemia: Clinical and Biochemical Features in Fifteen Kindreds

R. Lasker, A. Spiegel, S. Marx, 1981, Medicine.

Allelic deletions on chromosome 11q13 in multiple endocrine neoplasia type 1-associated and sporadic gastrinomas and pancreatic endocrine tumors.

F. Collins, L. Liotta, M. Emmert-Buck, 1997, Cancer research.

A transcript map for the 2.8-Mb region containing the multiple endocrine neoplasia type 1 locus.

B. Roe, M. Boguski, F. Collins, 1997, Genome research.

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

M. Merino, E. Friedman, P. Gejman, 1991, The New England journal of medicine.

The gene for multiple endocrine neoplasia type 1: recent findings.

F. Collins, L. Liotta, M. Emmert-Buck, 1999, Bone.

Abnormalities in G protein-coupled signal transduction pathways in human disease.

L. Weinstein, A. Shenker, A. Spiegel, 1993, The Journal of clinical investigation.

A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors.

F. Collins, M. Emmert-Buck, S. Libutti, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Somatic mutations of the MEN1 tumor suppressor gene in sporadic gastrinomas and insulinomas.

F. Collins, M. Emmert-Buck, A. Vortmeyer, 1997, Cancer research.

Aspiration of enlarged parathyroid glands for parathyroid hormone assay.

M. E. Brennan, J. Norton, J. Doppman, 1983, Radiology.

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

Y. Nakamura, K. Sakaguchi, E. Friedman, 1989, The New England journal of medicine.

Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states.

F. Collins, L. Liotta, M. Emmert-Buck, 1997, Human molecular genetics.

Albright's hereditary osteodystrophy and defective G proteins.

A. Spiegel, A. M. Spiegel, 1990, The New England journal of medicine.

Multiple facial angiofibromas and collagenomas in patients with multiple endocrine neoplasia type 1.

S. Steinberg, M. Turner, M. Skarulis, 1997, Archives of dermatology.

Bidirectional transcriptional activity of PGK‐neomycin and unexpected embryonic lethality in heterozygote chimeric knockout mice

J. Crabtree, P. Scacheri, S. Chandrasekharappa, 2001, Genesis.

Parathyroid adenomas in the aortopulmonary window.

J. Norton, J. Doppman, D. Fraker, 1996, Radiology.

Familial hypocalciuric hypercalcemia. The relation to primary parathyroid hyperplasia

R. Lasker, A. Spiegel, S. Marx, 1982 .

Neonatal primary hyperparathyroidism with autosomal dominant inheritance.

E. Brown, A. Spiegel, S. Marx, 1977, The Journal of pediatrics.

Regulation of guanine nucleotide binding regulatory proteins in cultured adrenal cells by adrenocorticotropin and angiotensin-II.

A. Spiegel, J. Saez, M. Bégeot, 1991, Endocrinology.

Journal of Clinical Endocrinology and Metabolism Printed in U.S.A. Copyright © 1998 by The Endocrine Society Treatment of Hypercalcemia Secondary to Parathyroid Carcinoma with a Novel Calcimimetic Agent

S. Silverberg, J. Bilezikian, M. Skarulis, 1997 .

An activating Gs alpha mutation is present in fibrous dysplasia of bone in the McCune-Albright syndrome.

L. Weinstein, A. Shenker, A. Spiegel, 1994, The Journal of clinical endocrinology and metabolism.

Receptor-effector coupling by G proteins: implications for normal and abnormal signal transduction.

L. Weinstein, A. Shenker, A. Spiegel, 1992, Endocrine reviews.

A prospective trial evaluating a standard approach to reoperation for missed parathyroid adenoma.

J. Norton, T. Shawker, J. Doppman, 1996, Annals of surgery.

The parathyroid/pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations.

F. Collins, W. Simonds, L. Weinstein, 2007, The Journal of clinical endocrinology and metabolism.

Multiple endocrine neoplasia type 1: clinical and genetic features of the hereditary endocrine neoplasias.

F. Collins, L. Liotta, M. Emmert-Buck, 1999, Recent progress in hormone research.

Identification of MEN1 gene mutations in sporadic carcinoid tumors of the lung.

F. Collins, L. Liotta, M. Emmert-Buck, 1997, Human molecular genetics.

MEN 1 Gene Analysis in Sporadic Adrenocortical Neoplasms *

B. Allolio, A. Burns, A. Spiegel, 1998 .

A heterozygous 4-bp deletion mutation in the Gs alpha gene (GNAS1) in a patient with Albright hereditary osteodystrophy.

P. Gejman, P. de Mazancourt, L. Weinstein, 1992, Genomics.

Gland Size Is Associated With Changes in Gene Expression Profiles in Sporadic Parathyroid Adenomas

S. Libutti, H. Alexander, H. Alexander, 2004, Annals of Surgical Oncology.

Familial hypocalciuric hypercalcemia: recognition among patients referred after unsuccessful parathyroid exploration.

J. Doppman, E. Brown, M. Brennan, 1980, Annals of internal medicine.

Loss of heterozygosity at 11q13: analysis of pituitary tumors, lung carcinoids, lipomas, and other uncommon tumors in subjects with familial multiple endocrine neoplasia type 1.

F. Collins, L. Liotta, M. Emmert-Buck, 1997, The Journal of clinical endocrinology and metabolism.

Menin molecular interactions: insights into normal functions and tumorigenesis.

F. Collins, S. Libutti, B. Oliver, 2005, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

Circulating parathyroid hormone activity: familial hypocalciuric hypercalcemia versus typical primary hyperparathyroidism.

E. Brown, D. Gardner, A. Spiegel, 1978, The Journal of clinical endocrinology and metabolism.

Mutations in G proteins and G protein-coupled receptors in endocrine disease.

A. Spiegel, A. M. Spiegel, 1996, The Journal of clinical endocrinology and metabolism.

Functional Effects of Monoclonal Antibodies to the Purified Amino‐Terminal Extracellular Domain of the Human Ca2+ Receptor

Jeffery L. Miller, Jianxin Hu, P. Goldsmith, 2007, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Autosomal Dominant Hypocalcemia Caused by a Novel Mutation in the Loop 2 Region of the Human Calcium Receptor Extracellular Domain

G. Colussi, M. E. De Ferrari, S. Mora, 2002, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Haplotype analysis defines a minimal interval for the multiple endocrine neoplasia type 1 (MEN1) gene.

F. Collins, L. Liotta, M. Emmert-Buck, 1997, Cancer research.

The G protein coupled to the thromboxane A2 receptor in human platelets is a member of the novel Gq family.

A. Shenker, A. Spiegel, P. Goldsmith, 1991, Transactions of the Association of American Physicians.

A 2.8-Mb clone contig of the multiple endocrine neoplasia type 1 (MEN1) region at 11q13.

B. Roe, A. C. Chinault, M. Boguski, 1997, Genomics.

Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein GS.

M. Merino, L. Weinstein, A. Shenker, 1993, The Journal of pediatrics.

Evidence for direct interaction of Gs alpha with the Ca2+ channel of skeletal muscle.

E. Stefani, S. Hamilton, L. Toro, 1991, The Journal of biological chemistry.

Urinary cAMP excretion during surgery: an index of successful parathyroidectomy in patients with primary hyperparathyroidism.

E. Brown, M. Brennan, A. Spiegel, 1978, The Journal of clinical endocrinology and metabolism.

Localization of the multiple endocrine neoplasia type I (MEN1) gene based on tumor loss of heterozygosity analysis.

F. Collins, L. Liotta, M. Emmert-Buck, 1997, Cancer research.

Allelic loss from chromosome 11 in parathyroid tumors.

J. Norton, E. Friedman, P. Gejman, 1992, Cancer research.

Deficient activity of guanine nucleotide regulatory protein in erythrocytes from patients with pseudohypoparathyroidism.

A. Spiegel, S. Marx, M. Levine, 1980, Biochemical and biophysical research communications.

Allelic deletions on chromosome 11q13 in multiple tumors from individual MEN1 patients.

F. Collins, L. Liotta, M. Emmert-Buck, 1996, Cancer research.

Germline and somatic mutation of the gene for multiple endocrine neoplasia type 1 (MEN1)

Kester, Manickam, I. Lubensky, 1998, Journal of internal medicine.

Maximal urine-concentrating ability: familial hypocalciuric hypercalcemia versus typical primary hyperparathyroidism.

A. Spiegel, S. Marx, M. Levine, 1981, The Journal of clinical endocrinology and metabolism.

Protein kinase C-mediated phosphorylation of retinal rod outer segment membrane proteins.

Y. Zick, L. Traub, A. Spiegel, 1989, Cellular signalling.