M H Meyer
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Explore the profile of M H Meyer including associated specialties, affiliations and a list of published articles.
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51
Citations
305
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Recent Articles
1.
Kiebzak G, Meyer M, Meyer Jr R
J Clin Densitom
. 2013 Apr;
2(1):17-21.
PMID: 23547309
The purpose of this study was to evaluate software from Lunar Corporation (Madison, WI) designed for the measurement of bone mineral content ([BMC],g) in excised rat femurs using dual-energy X-ray...
2.
Meyer R, Meyer M, Gray R, Brault B
Endocrine
. 2010 Dec;
3(3):209-14.
PMID: 21153196
YoungHyp mice malabsorb phosphate from the jejunum at 4 weeks of age. This has been attributed to both low plasma levels of 1,25-dihydroxyvitamin D and to intestinal resistance to stimulation...
3.
Meyer M, Letscher-Bru V, Waller J, Lutz P, Marcellin L, Herbrecht R
Clin Infect Dis
. 2002 Jun;
35(2):e22-5.
PMID: 12087540
We report a case of chronic disseminated Trichosporon asahii infection in a leukemic child. Administration of amphotericin B lipid complex resulted in rapid control and improvement of the initial infection...
4.
Meyer R, Meyer M, Phieffer L, Banks D
BMC Musculoskelet Disord
. 2001 Jul;
2:2.
PMID: 11454240
Background: Fracture healing slows with age. While 6-week-old rats regain normal bone biomechanics at 4 weeks after fracture, one-year-old rats require more than 26 weeks. The possible role of altered...
5.
Meyer M, Meyer Jr R
Endocrine
. 2000 Oct;
13(1):81-7.
PMID: 11051050
Phex is the gene whose mutation is the cause of X-linked hypophosphatemia in humans and mice. The organs expressing Phex in normal animals, and their possible sensitivity to stimulation by...
6.
Meyer Jr R, Young C, Meyer M, Garges P, Price D
Calcif Tissue Int
. 2000 Apr;
66(4):282-7.
PMID: 10742446
Pex is a newly discovered gene (also called Phex) whose mutation is the cause of X-linked hypophosphatemia. Other members of this gene family encode endopeptidases that activate or inactivate endocrine...
7.
Rude R, Kirchen M, Gruber H, Meyer M, Luck J, Crawford D
Magnes Res
. 1999 Dec;
12(4):257-67.
PMID: 10612083
Magnesium (Mg) intake has been linked to bone mass and/or rate of bone loss in humans. Experimental Mg deficiency in animal models has resulted in impaired bone growth, osteopenia, and...
8.
Thornton L, Meyer M, Meyer Jr R
Miner Electrolyte Metab
. 1999 Aug;
25(3):204-9.
PMID: 10436407
Hypophosphatemic (Hyp) mice have a reduced renal retention of phosphate. The beta-adrenergic agonist isoproterenol reverses phosphaturia induced by parathyroid hormone in the rat. This study determined whether isoproterenol could raise...
9.
Rude R, Kirchen M, Gruber H, Stasky A, Meyer M
Miner Electrolyte Metab
. 1998 Aug;
24(5):314-20.
PMID: 9705567
Disorders in which magnesium (Mg) depletion is common have an associated high incidence of osteoporosis. Mg depletion in humans results in hypocalcemia, low serum parathyroid hormone (PTH) and 1, 25(OH)2-vitamin...
10.
Meyer Jr R, Henley C, Meyer M, Morgan P, McDonald A, Mills C, et al.
Genomics
. 1998 Apr;
48(3):289-95.
PMID: 9545633
Gy, along with Hyp, is a dominant mutation of the normal gene Pex causing X-linked hypophosphatemia in the mouse. Hemizygous Gy male mice, however, have greater defects in survival, bodily...