191 Publications (Page 7 of 8)
2001
Hypophosphatemic Rickets
Di Meglio, Linda A and Econs, Michael
Reviews in Endocrine & Metabolic Disorders, vol. 2, (no. 2), pp. 165, Apr 2001. | Journal Article
 
Hypophosphatemic Rickets
DiMeglio, Linda⋅Di Meglio, Linda⋅Econs, Michael and Econs, Michael
Reviews in Endocrine and Metabolic Disorders, vol. 2, (no. 2), pp. 173, 20010400. | Journal Article
 
Hypophosphatemic Rickets
DiMeglio, Linda and Econs, Michael
Reviews in Endocrine & Metabolic Disorders, vol. 2, (no. 2), pp. 165-73, Apr 2001. | Journal Article
 
The autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wasting.
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The Autosomal Dominant Hypophosphatemic Rickets (ADHR) Gene Is a Secreted Polypeptide Overexpressed by Tumors that Cause Phosphate Wasting
White, Kenneth E⋅White, Kenneth E⋅Jonsson, Kenneth B⋅Jonsson, Kenneth B⋅Carn, Gwenaelle⋅Carn, Gwenaelle⋅Hampson, Geeta⋅Hampson, Geeta⋅Spector, Tim D⋅Spector, Tim D⋅Mannstadt, Michael⋅Mannstadt, Michael⋅Lorenz-Depiereux, Bettina⋅Lorenz-Depiereux, Bettina⋅Miyauchi, Akimitsu⋅Miyauchi, Akimitsu⋅Yang, In Myung⋅Yang, In Myung⋅Ljunggren, Östen⋅Ljunggren, Östen⋅Meitinger, Thomas⋅Meitinger, Thomas⋅Strom, Tim M⋅Strom, Tim M⋅Jüppner, Harald⋅Jüppner, Harald⋅Econs, Michael J and Econs, Michael J
The Journal of Clinical Endocrinology & Metabolism, vol. 86, (no. 2), pp. 500, 2001-02. | Journal Article
2000
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
White, Kenneth E⋅Evans, Wayne E⋅O'Riordan, Jeffery L⋅Speer, Marcy C⋅Econs, Michael⋅Lorenz-Depiereux, Bettina⋅Grabowski, Monika⋅Meitinger, Thomas and Strom, Tim M
Nature Genetics, vol. 26, (no. 3), pp. 345-348, Nov 2000. | Journal Article
 
DISORDERS OF PHOSPHATE METABOLISM
Di Meglio, Linda A⋅DiMeglio, Linda A⋅DiMeglio, Linda A⋅White, Kenneth E⋅White, Kenneth E⋅White, Kenneth E⋅Econs, Michael J⋅Econs, Michael J and Econs, Michael J
Endocrinology and Metabolism Clinics of North America, vol. 29, (no. 3), pp. 609, 2000. | Journal Article
 
Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis.
Koller, Daniel⋅Econs, Michael J⋅Morin, Phillip A⋅Christian, Joe C⋅Hui, Siu L⋅Parry, P⋅Curran, M E⋅Rodriguez, L A⋅Conneally, P. M⋅Joslyn, G⋅Peacock, Munro⋅Johnston, C C and Foroud, Tatiana M
The Journal of clinical endocrinology and metabolism, vol. 85, (no. 9), pp. 3116-20, 2000/Sep. | Journal Article
 
Heterogeneity in Paget disease of the bone
Nance, Martha A⋅Nuttall, Frank Q⋅Econs, Michael J⋅Lyles, Kenneth W⋅Viles, Kristi D⋅Vance, Jeffery M⋅Pericak‐Vance, Margaret A and Speer, Marcy C
American Journal of Medical Genetics, vol. 92, (no. 5), pp. 307, 19 June 2000. | Journal Article
 
MEPE, a New Gene Expressed in Bone Marrow and Tumors Causing Osteomalacia
Rowe, PSN⋅de Zoysa, PA⋅Dong, Rong⋅Wang, Huei R⋅White, Kenneth E⋅Econs, Michael and Oudet, CL
Genomics, vol. 67, (no. 1), pp. 54-68, 2000. | Journal Article
 
Molecular cloning of a novel human UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase, GalNAc-T8, and analysis as a candidate autosomal dominant hypophosphatemic rickets (ADHR) gene
White, Kenneth E⋅Lorenz, Bettina⋅Evans, Wayne E⋅Meitinger, Thomas⋅Strom, Tim M and Econs, Michael J
Gene, vol. 246, (no. 1), pp. 356, 2000. | Journal Article
 
Sib pair linkage and association studies between bone mineral density and the interleukin-6 gene locus.
Takacs, I⋅Koller, Daniel⋅Peacock, Munro⋅Christian, J C⋅Evans, W E⋅Hui, Siu L⋅Conneally, P M⋅Johnston, C C⋅Foroud, T and Econs, M J
. | Journal Article
1999
Bone Mineral Density and Laboratory Evaluation of a Type II Autosomal Dominant Osteopetrosis Carrier
Takacs, I.⋅Cooper, H.⋅Weaver, David D and Econs, Michael
American Journal of Medical Genetics, vol. 85, (no. 1), pp. 9-12, 1999. | Journal Article
 
Locus heterogeneity of autosomal dominant osteopetrosis (ADO).
White, Kenneth E⋅Koller, Daniel⋅Takacs, I⋅Buckwalter, Kenneth A⋅Foroud, Tatiana M and Econs, Michael J
The Journal of clinical endocrinology and metabolism, vol. 84, (no. 3), pp. 1047-51, 1999/Mar. | Journal Article
 
Locus Heterogeneity of Autosomal Dominant Osteopetrosis (ADO)1
White, Kenneth E⋅White, Kenneth E⋅White, Kenneth E⋅White, Kenneth E⋅Koller, Daniel L⋅Koller, Daniel L⋅Koller, Daniel L⋅Koller, Daniel L⋅Takacs, Istvan⋅Takacs, Istvan⋅Takacs, Istvan⋅Takacs, Istvan⋅Buckwalter, Kenneth A⋅Buckwalter, Kenneth A⋅Buckwalter, Kenneth A⋅Buckwalter, Kenneth A⋅Foroud, Tatiana⋅Foroud, Tatiana⋅Foroud, Tatiana⋅Foroud, Tatiana⋅Econs, Michael J⋅Econs, Michael J⋅Econs, Michael J and Econs, Michael J
The Journal of Clinical Endocrinology & Metabolism, vol. 84, (no. 3), pp. 1051, 1999-03. | Journal Article
 
New insights into the pathogenesis of inherited phosphate wasting disorders.
Econs, Michael J
Bone. , vol. 25, (no. 1), pp. 131-5, 1999/Jul. | Journal Article
 
Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues.
Filisetti, D⋅Ostermann, G⋅von Bredow, M⋅Strom, Terry B⋅Filler, G⋅Ehrich, J⋅Pannetier, S⋅Garnier, J M⋅Rowe, Peter S. N⋅Francis, F⋅Julienne, A⋅Hanauer, A⋅Econs, M J and Oudet, C
. | Journal Article
 
Osteopathia Striata with Cranial Sclerosis
Lazar, Cristina M⋅Braunstein, Ethan M and Econs, Michael J
Journal of Bone and Mineral Research, vol. 14, (no. 1), pp. 153, January 1999. | Journal Article
 
Sibling Pair Linkage and Association Studies between Bone Mineral Density and the Insulin-Like Growth Factor I Gene Locus
Takacs, I.⋅Koller, Daniel⋅Peacock, Munro⋅Christian, Joe C⋅Hui, Siu L⋅Conneally, P. M⋅Johnston, CC J⋅Foroud, Tatiana M and Econs, Michael
Journal of Clinical Endocrinology and Metabolism, vol. 84, (no. 12), pp. 4467-4471, 1999. | Journal Article
 
Sibling Pair Linkage and Association Studies between Bone Mineral Density and the Insulin-Like Growth Factor I Gene Locus1
Takacs, Istvan⋅Takacs, Istvan⋅Takacs, Istvan⋅Koller, Daniel L⋅Koller, Daniel L⋅Koller, Daniel L⋅Peacock, Munro⋅Peacock, Munro⋅Peacock, Munro⋅Christian, Joe C⋅Christian, Joe C⋅Christian, Joe C⋅Hui, Siu L⋅Hui, Siu L⋅Hui, Siu L⋅Conneally, P. Michael⋅Conneally, P. Michael⋅Conneally, P. Michael⋅Johnston, C. Conrad⋅Johnston, C. Conrad⋅Johnston, C. Conrad⋅Foroud, Tatiana⋅Foroud, Tatiana⋅Foroud, Tatiana⋅Econs, Michael J⋅Econs, Michael J and Econs, Michael J
The Journal of Clinical Endocrinology & Metabolism, vol. 84, (no. 12), pp. 4471, 1999-12. | Journal Article
1998
A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia: evidence that the disorder is not a distinct entity from X-linked hypophosphatemic rickets.
Econs, Michael J⋅Friedman, Nancy E⋅Rowe, P S⋅Speer, M C⋅Francis, F⋅Strom, T M⋅Oudet, C⋅Smith, J A⋅Ninomiya, J T⋅Lee, B E and Bergen, H
The Journal of clinical endocrinology and metabolism, vol. 83, (no. 10), pp. 3459-62, 1998/Oct. | Journal Article
 
A PHEX Gene Mutation Is Responsible for Adult-Onset Vitamin D-Resistant Hypophosphatemic Osteomalacia: Evidence That the Disorder Is Not a Distinct Entity from X-Linked Hypophosphatemic Rickets1
Econs, Michael J⋅Friedman, Nancy E⋅Rowe, Peter S. N⋅Speer, Marcy C⋅Francis, Fiona⋅Strom, Tim M⋅Oudet, Claudine⋅Smith, John A⋅Ninomiya, James T⋅Lee, Benjamin E and Bergen, Heather
The Journal of Clinical Endocrinology & Metabolism, vol. 83, (no. 10), pp. 3462, 1998-10. | Journal Article
 
Chromosomal localization of two human genes involved in phosphate homeostasis: the type IIb sodium-phosphate cotransporter and stanniocalcin-2.
White, Kenneth E⋅Biber, J⋅Murer, H and Econs, Michael J
Somatic cell and molecular genetics, vol. 24, (no. 6), pp. 357-62, 1998/Nov. | Journal Article
 
Linkage of a QTL contributing to normal variation in bone mineral density to chromosome 11q12-13.
Koller, Daniel⋅Rodriguez, L A⋅Christian, Joe C⋅Slemenda, Charles W⋅Econs, Michael J⋅Hui, Siu L⋅Morin, Phillip A⋅Conneally, P. M⋅Joslyn, G⋅Curran, M E⋅Peacock, Munro⋅Johnston, C C and Foroud, Tatiana M
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, vol. 13, (no. 12), pp. 1903-8, 1998/Dec. | Journal Article
 
Localization of PiUS, a stimulator of cellular phosphate uptake to human chromosome 3p21.3
White, Kenneth and Econs, Michael
Somatic Cell and Molecular Genetics, vol. 24, (no. 1), pp. 74, 19980100. | Journal Article