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59篇 您的检索式:作者名="Whyte MP"
    题名 作者 年代 出处 被引量
1Desctivating germline mutations in LEMD3 cause osteopoililu- sis and Buschke-Ollendorff syndrome, but not sporadic melorheos- tosis显示文摘Mumm S Wenkert D Zhang X McAlister WH Mier RJ Whyte MP 2007J Bone Miner Res2007,22,2:1
2Infantile hypophos-phatasia:enzyme replacement therapy by intravenous infusion ofalkaline phosphatase-rich plasma from patients with Paget bonedisease显示文摘Whyte MP Valdes R Jr Ryan LM 1982J Pediatr1982,101,3:1
3Enzyme replacementtherapy for infantile hypophosphatasia attempted by intravenousinfusions of alkaline phosphatase-rich Paget plasma:results inthree additional patients显示文摘Whyte MP McAlister WH Patton LS 1984J Pediatr1984,105,:1
4X-linked recessive spondyloepiphyseal dysplasia tarda显示文摘Whyte MP Gottesman GS Eddy MC 0,,:1
5Hypophosphatasia and the role of alkaline phospha-tase in skeletal mineralization 显示文摘Whyte MP 1994Endocr Rev1994,15,4:1
6Enzyme-replacement therapy in life-threatening hypophosphatasia显示文摘Whyte MP Greenberg CR Salman NJ 2012N Engl J Med2012,366,:1
7Adult hypophosphatasia treated with teriparatide显示文摘Whyte MP Mumm S Deal C 2007J Clin Endocrinol Metab2007,92,:1
8Tibial bowing exacerbated by partial premature epiphyseal closure in sex-linked hypophosphatamic rickets显示文摘Mcalister WH Kim GS Whyte MP 1987Radiology1987,162,:1
9Pregnancy-associated oste-oporosis with a heterozygous deactivating LDL receptor-related protein 5(LRPS) mutation and a homozygous methylenetetrahy- drofolate reductase (MTHFR) polymorphism 显示文摘Cook FJ Mumm S Whyte MP 2014J Bone Miner Res2014,29,4:1
10Hypophosphatasia and the extracellular metabolism of inorganic pyrophos- phate: clinical and laboratory aspects 显示文摘Caswell A Whyte MP Russell RG 1991Crit Rev Clin Lab Sci1991,28,3:1
11Marrow cell transplantation for infantile hypophosphatasia 显示文摘Whyte MP Kurtzberg J McAlister WH 2003J Bone Miner Res2003,18,4:1
12Absence of parathyroid tissue in sex-linked recessive hypoparathyroidism 显示文摘Whyte MP Kim GS Kosanovieh M 1986J Pediatr1986,109,5:1
13Alendronate for the treatment of pediatric osteogcnesis imperfecta : A randomized placebo-controlled study 显示文摘Ward LM Rauch F Whyte MP 2011J Clin Endocrinol Metab2011,96,2:1
14Acute severe hypercalcemia after ffaumatic fractures and immobilization in hypophosphatasia complicated by chronic renal failure 显示文摘Whyte MP Leelawattana R Reinus WR 2013J Clin Endocrinol Metab2013,98,12:1
15The carbonic anhydrase Ⅱ deficiency syndrome : osteopetrosis with renal tubular acidosis and cerebral calcification显示文摘Sly WS Whyte MP Sundaram V 1985N Engl J Med1985,313,3:1
16Severe hypophatemia in children with kwashiorkor is associated with increased mortality显示文摘Manary M J Hart CA Whyte MP 1998J Pediatr1998,133,6:1
17Inclusion body myopathy associ- ated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein 显示文摘Pestronk A Whyte MP Kimonis VE 2004Nat Genet2004,36,4:1
18Skeletal fluorosis and instant tea显示文摘Whyte MP Essmyer K Gannon FH etal 2005Am J Med2005,118,:1
19Skeletal fluorosis and instant tea显示文摘Whyte MP Essmyer K Gannon FH 2005Am J Med2005,118,:1
20Osteoprote- gerin deficiency and juvenile Paget's disease 显示文摘Whyte MP Obrecht SE Finnegan PM 2002N Engl J Med2002,347,:1
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