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	1.	Heritable disorders of the RANKL/OPG/RANK signaling pathway. [electronic resource] by Whyte, Michael P Mumm, Steven Producer: 20050124 In: Journal of musculoskeletal & neuronal interactions vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	2.	Adult hypophosphatasia treated with teriparatide. [electronic resource] by Whyte, Michael P Mumm, Steven Deal, Chad Producer: 20070917 In: The Journal of clinical endocrinology and metabolism vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	High-bone-mass disease and LRP5. [electronic resource] by Whyte, Michael P Reinus, William H Mumm, Steven Producer: 20040517 In: The New England journal of medicine vol. 350 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Low serum alkaline phosphatase activity and pathologic fracture: case report and brief review of hypophosphatasia diagnosed in adulthood. [electronic resource] by Khandwala, Hasnain M Mumm, Steven Whyte, Michael P Producer: 20070307 In: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Homozygosity for TNSALP mutation 1348c>T (Arg433Cys) causes infantile hypophosphatasia manifesting transient disease correction and variably lethal outcome in a kindred of black ancestry. [electronic resource] by Whyte, Michael P Essmyer, Kevan Geimer, Michael Mumm, Steven Producer: 20060726 In: The Journal of pediatrics vol. 148 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Pregnancy-associated osteoporosis with a heterozygous deactivating LDL receptor-related protein 5 (LRP5) mutation and a homozygous methylenetetrahydrofolate reductase (MTHFR) polymorphism. [electronic resource] by Cook, Fiona J Mumm, Steven Whyte, Michael P Wenkert, Deborah Producer: 20141203 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Oropharyngeal skeletal disease accompanying high bone mass and novel LRP5 mutation. [electronic resource] by Rickels, Michael R Zhang, Xiafang Mumm, Steven Whyte, Michael P Producer: 20050819 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Absence of MMP2 mutation in idiopathic multicentric osteolysis with nephropathy. [electronic resource] by Wenkert, Deborah Mumm, Steven Wiegand, Stefanie M McAlister, William H Whyte, Michael P Producer: 20071101 In: Clinical orthopaedics and related research vol. 462 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Bisphosphonate-induced osteopetrosis. [electronic resource] by Whyte, Michael P Wenkert, Deborah Clements, Karen L McAlister, William H Mumm, Steven Producer: 20030804 In: The New England journal of medicine vol. 349 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Juvenile paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutation. [electronic resource] by Saki, Forough Karamizadeh, Zohreh Nasirabadi, Shiva Mumm, Steven McAlister, William H Whyte, Michael P Producer: 20131209 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	ADULT HYPOPHOSPHATASIA TREATED WITH TERIPARATIDE: REPORT OF 2 PATIENTS AND REVIEW OF THE LITERATURE. [electronic resource] by Camacho, Pauline M Mazhari, Alaleh M Wilczynski, Cory Kadanoff, Ruth Mumm, Steven Whyte, Michael P Producer: 20170523 In: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Deactivating germline mutations in LEMD3 cause osteopoikilosis and Buschke-Ollendorff syndrome, but not sporadic melorheostosis. [electronic resource] by Mumm, Steven Wenkert, Deborah Zhang, Xiafang McAlister, William H Mier, Richard J Whyte, Michael P Producer: 20070320 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Elevated serum lactate dehydrogenase isoenzymes and aspartate transaminase distinguish Albers-Schönberg disease (Chloride Channel 7 Deficiency Osteopetrosis) among the sclerosing bone disorders. [electronic resource] by Whyte, Michael P Kempa, Lydia G McAlister, William H Zhang, Fan Mumm, Steven Wenkert, Deborah Producer: 20110209 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Denaturing gradient gel electrophoresis analysis of the tissue nonspecific alkaline phosphatase isoenzyme gene in hypophosphatasia. [electronic resource] by Mumm, Steven Jones, Jonathan Finnegan, Patrick Henthorn, Paula S Podgornik, Michelle N Whyte, Michael P Producer: 20020521 In: Molecular genetics and metabolism vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	"Atypical femoral fractures" during bisphosphonate exposure in adult hypophosphatasia. [electronic resource] by Sutton, Roger A L Mumm, Steven Coburn, Stephen P Ericson, Karen L Whyte, Michael P Producer: 20120927 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Acute severe hypercalcemia after traumatic fractures and immobilization in hypophosphatasia complicated by chronic renal failure. [electronic resource] by Whyte, Michael P Leelawattana, Rattana Reinus, William R Yang, Chang Mumm, Steven Novack, Deborah V Producer: 20140414 In: The Journal of clinical endocrinology and metabolism vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Fibrodysplasia ossificans progressiva: middle-age onset of heterotopic ossification from a unique missense mutation (c.974G>C, p.G325A) in ACVR1. [electronic resource] by Whyte, Michael P Wenkert, Deborah Demertzis, Jennifer L DiCarlo, Edward F Westenberg, Erica Mumm, Steven Producer: 20120718 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand. [electronic resource] by Whyte, Michael P Totty, William G Novack, Deborah V Zhang, Xiafang Wenkert, Deborah Mumm, Steven Producer: 20110817 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Lenz-Majewski hyperostotic dwarfism with hyperphosphoserinuria from a novel mutation in PTDSS1 encoding phosphatidylserine synthase 1. [electronic resource] by Whyte, Michael P Blythe, Amanda McAlister, William H Nenninger, Angela R Bijanki, Vinieth N Mumm, Steven Producer: 20160108 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Genes and translocations involved in POF. [electronic resource] by Schlessinger, David Herrera, Luisa Crisponi, Laura Mumm, Steven Percesepe, Antonio Pellegrini, Massimo Pilia, Giuseppe Forabosco, Antonino Producer: 20030212 In: American journal of medical genetics vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 61 results.