X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1943) 1943
Book Review (537) 537
Publication (121) 121
Book / eBook (65) 65
Book Chapter (40) 40
Conference Proceeding (2) 2
Reference (2) 2
Data Set (1) 1
Dissertation (1) 1
Magazine Article (1) 1
Newspaper Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (1551) 1551
humans (1499) 1499
male (674) 674
female (670) 670
mutation (541) 541
middle aged (496) 496
adult (474) 474
amyloidosis (451) 451
aged (357) 357
biochemistry & molecular biology (300) 300
neurosciences (265) 265
hereditary amyloidosis (256) 256
amyloidosis - genetics (238) 238
hereditary cerebral-hemorrhage (230) 230
genetic aspects (228) 228
animals (224) 224
transthyretin (224) 224
pedigree (218) 218
gene (208) 208
medicine, general & internal (207) 207
clinical neurology (202) 202
ophthalmology (197) 197
disease (182) 182
diagnosis (181) 181
corneal dystrophies, hereditary - genetics (177) 177
amyloid (169) 169
amyloidosis - pathology (169) 169
prealbumin - genetics (168) 168
polyneuropathy (167) 167
familial mediterranean fever (165) 165
alzheimer's disease (152) 152
corneal dystrophies, hereditary - pathology (152) 152
alzheimers-disease (151) 151
abridged index medicus (150) 150
medicine, research & experimental (146) 146
child (145) 145
phenotype (145) 145
pathology (141) 141
proteins (139) 139
adolescent (133) 133
protein (132) 132
genetics (128) 128
amyloid - metabolism (127) 127
genetics & heredity (127) 127
dna mutational analysis (121) 121
analysis (119) 119
molecular sequence data (119) 119
hereditary (118) 118
liver-transplantation (113) 113
hereditary diseases (111) 111
mutations (108) 108
rheumatology (105) 105
amino acid sequence (101) 101
medicine & public health (101) 101
research (101) 101
amyloidosis - metabolism (100) 100
aged, 80 and over (96) 96
fever (94) 94
point mutation (94) 94
amyloid neuropathies, familial - genetics (91) 91
diagnosis, differential (89) 89
familial amyloid polyneuropathy (89) 89
hereditary autoinflammatory diseases - genetics (89) 89
polymerase chain reaction (89) 89
systemic amyloidosis (88) 88
neuropathy (87) 87
biopsy (86) 86
mutation - genetics (86) 86
risk factors (86) 86
amyloidosis - diagnosis (85) 85
base sequence (85) 85
variant (85) 85
familial amyloidosis (84) 84
gene mutations (84) 84
genetic disorders (84) 84
genes (83) 83
cardiomyopathy (81) 81
immunohistochemistry (80) 80
amyloidosis - complications (78) 78
immunology (78) 78
liver transplantation (78) 78
mice (78) 78
diseases (76) 76
transplantation (76) 76
alzheimer disease - genetics (75) 75
amyloidosis, familial - genetics (75) 75
care and treatment (75) 75
neurology (75) 75
child, preschool (74) 74
gelsolin (73) 73
hereditary autoinflammatory diseases - diagnosis (72) 72
patients (72) 72
medicine (71) 71
syndrome (71) 71
cell biology (70) 70
hereditary renal amyloidosis (70) 70
article (69) 69
cardiac amyloidosis (69) 69
inflammation (69) 69
young adult (69) 69
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (51) 51
UTL at Downsview - May be requested (7) 7
UofT at Mississauga - Stacks (4) 4
Collection Dvlpm't (Acquisitions) - Closed Orders (3) 3
Holland Bloorview Kids Rehabilitation - Stacks (3) 3
Dentistry (Harry R Abbott) - Stacks (2) 2
Scarborough Hospital - Birchmount (2) 2
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (2) 2
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Dentistry (Harry R Abbott) - Withdrawn (1) 1
Gerstein Science - Reference (1) 1
Lakeridge Health Sciences - Oshawa (1) 1
Mt Sinai Hospital - Pathology (1) 1
Online Resources - Online (1) 1
Robarts - Stacks (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
St. Michael's Hospital - Stacks (1) 1
UofT at Scarborough - Stacks (1) 1
UofT at Scarborough - Sunnybrook Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1885) 1885
French (49) 49
German (47) 47
Spanish (23) 23
Japanese (14) 14
Chinese (6) 6
Hungarian (5) 5
Russian (5) 5
Finnish (4) 4
Portuguese (3) 3
Czech (2) 2
Turkish (2) 2
Arabic (1) 1
Dutch (1) 1
Polish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


REVISTA CLINICA ESPANOLA, ISSN 0014-2565, 04/2019, Volume 219, Issue 3, pp. 141 - 144
Background and objective: There are 2 types of amytoidosis caused by transthyretin deposits: the wild type (wt-ATTR) and the mutant type (m-ATTR), transmitted... 
DIAGNOSIS | MEDICINE, GENERAL & INTERNAL | MANAGEMENT | Cardiomyopathy | Hereditary amytoidosis | Transthyretin | Heterogeneous disease | MUTATION | DISEASE | COMMON | Polyneuropathy | CARDIAC AMYLOIDOSIS
Journal Article
PLoS One, ISSN 1932-6203, 2013, Volume 8, Issue 10, pp. e75242 - e75242
Journal Article
European Journal of Medical Genetics, ISSN 1769-7212, 2015, Volume 58, Issue 4, pp. 211 - 215
Journal Article
Medicine (United States), ISSN 0025-7974, 03/2017, Volume 96, Issue 10
Rationale: Hereditary amyloidosis is diagnosed worldwidely with an increasing incidence. As the most common form, transthyretin-related hereditary amyloidosis... 
case report | p.Leu75Pro | transthyretin-related hereditary amyloidosis | rs121918079 | renal insufficiency | TTR mutation | MEDICINE, GENERAL & INTERNAL | POLYNEUROPATHY | LIVER-TRANSPLANTATION | INVOLVEMENT | DISEASE | KIDNEY
Journal Article
Medical Journal of Wuhan University, ISSN 1671-8852, 11/2017, Volume 38, Issue 6, pp. 1013 - 1015
Journal Article
Journal of Molecular Biology, ISSN 0022-2836, 2005, Volume 352, Issue 4, pp. 823 - 836
Journal Article
AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS, ISSN 1350-6129, 2015, Volume 22, Issue 4, pp. 210 - 220
Journal Article
Journal Article
Medizinische Klinik, ISSN 0723-5003, 2008, Volume 103, Issue 3, pp. 153 - 160
Journal Article
Amyloid, ISSN 1350-6129, 01/2019, Volume 26, Issue 1, pp. 3 - 9
Diagnosis in the early stages of hereditary transthyretin (ATTR) amyloidosis is imperative to support timely treatment to prevent or delay disease progression.... 
minimum criteria for diagnosis | carrier | amyloidosis | predicted age of disease onset | transthyretin | diagnosis | hereditary | ATTR | follow up | MEDICINE, RESEARCH & EXPERIMENTAL | MANAGEMENT | BIOCHEMISTRY & MOLECULAR BIOLOGY | MEDICINE, GENERAL & INTERNAL | VAL30MET MUTATION
Journal Article