ライフサイエンスコーパス: Paget's disease

1 ontribute to the elevated numbers of OCLs in Paget's disease.

2 static and nonmetastatic prostate cancer and Paget's disease.

3 Juvenile Paget's disease, an autosomal recessive osteopathy, is c

4 ave been identified in four genes that cause Paget's disease and related syndromes.

5 asts are valuable for treating osteoporosis, Paget's disease, and inflammation of bone associated wit

6 ral" diseases such as multiple sclerosis and Paget's disease, and the controversy surrounding MV vacc

7 Osteoclasts (OCLs) in Paget's disease are markedly increased in number and siz

8 oviding evidence for an epidermal origin for Paget's disease, as well as a high incidence of mutation

9 protegerin deficiency could explain juvenile Paget's disease because osteoprotegerin suppresses bone

10 destruction in postmenopausal osteoporosis, Paget's disease, bone metastasis, and hypercalcemia of m

11 Recognizing that Paget's disease can not only cause absent but also expan

12 Juvenile Paget's disease can result from osteoprotegerin deficien

13 as been used in therapy for osteoporosis and Paget's disease for decades, human calcitonin (hCT) form

14 ntly unrelated Navajo patients with juvenile Paget's disease for defects in the gene encoding osteopr

15 (2018) bring Paget's disease into the genomics era, providing evidenc

16 Paget's disease is characterized by highly localized are

17 Paget's disease is often asymptomatic but can be associa

18 ride therapy (n = 20) and patients with mild Paget's disease (n = 5).

19 ations in the VCP gene, results in myopathy, Paget's disease of bone (PBD) and frontotemporal dementi

20 Paget's disease of bone (PDB) is a chronic skeletal diso

21 Paget's disease of bone (PDB) is a common disorder chara

22 Paget's disease of bone (PDB) is a common disorder chara

23 Paget's disease of bone (PDB) is a common disorder with

24 Paget's disease of bone (PDB) is a common disorder with

25 Paget's disease of bone (PDB) is characterised by focal

26 Paget's disease of bone (PDB) is characterized by focal

27 Paget's disease of bone (PDB) is the second most common

28 with numerous neurodegenerative diseases and Paget's disease of bone (PDB), a degenerative bone disea

29 of SQSTM1 occur in about10% of patients with Paget's disease of bone (PDB), but it is unclear whether

30 the mutations of which lead to rare forms of Paget's disease of bone (PDB)-like syndrome-such as incl

31 hy (IBM), frontotemporal dementia (FTD), and Paget's disease of bone (PDB).

32 Patients with SQSTM1 mutations have severe Paget's disease of bone and a high degree of penetrance

33 Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBM

34 Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBM

35 m patients with inclusion body myopathy with Paget's disease of bone and frontotemporal dementia (IBM

36 nclusion body myopathy (IBM) associated with Paget's disease of bone and frontotemporal dementia (IBM

37 ding p62 are commonly found in patients with Paget's disease of bone and largely cluster within the C

38 Paget's disease of bone is a common disease characterise

39 Medical management of Paget's disease of bone is based on giving inhibitors of

40 We report a case of polyostotic Paget's disease of bone that caused an unusual pattern o

41 mutant that causes inclusion body myopathy, Paget's disease of bone, and frontotemporal dementia in

42 prevent the development of complications of Paget's disease of bone, and further work is needed to a

43 , including cancer-related hypercalcemia and Paget's disease of bone, studies have been initiated to

44 , including cancer-related hypercalcemia and Paget's disease of bone, studies were initiated to explo

45 e treatment of osteopenia, osteoporosis, and Paget's disease of bone.

46 are a common cause of familial and sporadic Paget's disease of bone.

47 eat osteoporosis in postmenopausal women and Paget's disease of bone.

48 flict two families, mainly with myopathy and Paget's disease of bone.

49 stm1/p62 whose mutations have been linked to Paget's disease of bone.

50 Inclusion body myopathy associated with Paget's disease of the bone and fronto-temporal dementia

51 ted syndrome of inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia

52 ause inclusion body myopathy associated with Paget's disease of the bone and frontotemporal dementia

53 es that include inclusion body myopathy with Paget's disease of the bone and frontotemporal dementia,

54 n as inclusion body myopathy associated with Paget's disease of the bone and frontotemporal dementia.

55 ns are the cause of inclusion body myopathy, Paget's disease of the bone, and frontotemporal dementia

56 n (VCP) cause inclusion body myopathy (IBM), Paget's disease of the bone, and frontotemporal dementia

57 henotypes including inclusion body myopathy, Paget's disease of the bone, and frontotemporal dementia

58 nclusion body myopathy (IBM) associated with Paget's disease of the bone, fronto-temporal dementia an

59 insonism, frontotemporal dementia, myopathy, Paget's disease, or a combination of these.

60 rugs used in the treatment of hypercalcemia, Paget's disease, osteoporosis, and malignancy.

61 Paget's disease (PD) is characterized by focal and drama

62 e molecular etiology and cellular origins of Paget's disease remain poorly understood.

63 This case suggests that Paget's disease should be considered as a diagnostic pos

64 ugs that treat osteoporosis, hypercalcaemia, Paget's disease, type II diabetes, and obesity and are b

65 role of MV in the abnormal OCL phenotype of Paget's disease, we transduced normal OCL precursors wit

66 e yields samples which permit a diagnosis of Paget's disease without surgical biopsy.