UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
pseudohypoparathyroidism (115) 115
albright hereditary osteodystrophy (104) 104
humans (91) 91
life sciences & biomedicine (85) 85
science & technology (85) 85
albright's hereditary osteodystrophy (68) 68
female (59) 59
male (50) 50
gtp-binding protein alpha subunits, gs - genetics (44) 44
child (36) 36
pseudohypoparathyroidism - genetics (36) 36
pseudopseudohypoparathyroidism (33) 33
adolescent (32) 32
genetics & heredity (30) 30
gnas (30) 30
mutation (30) 30
endocrinology & metabolism (27) 27
parathyroid hormone (26) 26
chromogranins (25) 25
fibrous dysplasia, polyostotic - genetics (24) 24
pediatrics (23) 23
adult (21) 21
albright’s hereditary osteodystrophy (21) 21
child, preschool (21) 21
phenotype (20) 20
progressive osseous heteroplasia (19) 19
brachydactyly (17) 17
pseudohypoparathyroidism - diagnosis (17) 17
case report (16) 16
pedigree (16) 16
imprinting (15) 15
infant (15) 15
pseudohypoparathyroidism - complications (15) 15
musculoskeletal diseases (14) 14
osteoma cutis (14) 14
genetic aspects (13) 13
genomic imprinting (12) 12
heterozygote (12) 12
gnas gene (11) 11
gnas1 (11) 11
pseudohypoparathyroidism type ia (11) 11
chromosome deletion (10) 10
hypocalcaemia (10) 10
hypocalcemia (10) 10
mutation - genetics (10) 10
pseudohypoparathyroidism - blood (10) 10
radiography (10) 10
diagnosis (9) 9
hypothyroidism (9) 9
obesity (9) 9
pseudopseudohypoparathyroidism - genetics (9) 9
acrodysostosis (8) 8
animals (8) 8
chromogranins - genetics (8) 8
genetics (8) 8
hormone resistance (8) 8
methylation (8) 8
middle aged (8) 8
ossification, heterotopic - pathology (8) 8
osteodystrophy (8) 8
pseudo-pseudohypoparathyroidism (8) 8
chromosomes, human, pair 2 - genetics (7) 7
diagnosis, differential (7) 7
fibrous dysplasia, polyostotic - diagnosis (7) 7
heterotopic ossification (7) 7
hypoparathyroidism (7) 7
internal medicine (7) 7
medicine (7) 7
ossification, heterotopic - genetics (7) 7
patients (7) 7
proteins (7) 7
signal transduction (7) 7
syndrome (7) 7
aho (6) 6
albright hereditary osteodystrophy-like syndrome (6) 6
body height (6) 6
calcium (6) 6
calcium - blood (6) 6
children (6) 6
dna mutational analysis (6) 6
fibrodysplasia ossificans progressiva (6) 6
fibrous dysplasia, polyostotic - complications (6) 6
g proteins (6) 6
hyperphosphatemia (6) 6
medicine, general & internal (6) 6
research (6) 6
short stature (6) 6
brachydactyly - genetics (5) 5
care and treatment (5) 5
cutaneous ossification (5) 5
dermatology (5) 5
dna methylation (5) 5
endocrinology (5) 5
fibrous dysplasia, polyostotic - diagnostic imaging (5) 5
general & internal medicine (5) 5
genetic testing (5) 5
genotype & phenotype (5) 5
gtp-binding protein alpha subunits, gs - metabolism (5) 5
intellectual disability - genetics (5) 5
medicine & public health (5) 5
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (172) 172
French (8) 8
Spanish (6) 6
German (5) 5
Japanese (4) 4
Czech (2) 2
Korean (2) 2
Portuguese (2) 2
Italian (1) 1
Russian (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Frontiers in endocrinology (Lausanne), ISSN 1664-2392, 08/2019, Volume 10
Pseudohypoparathyroidism (PHP) is a rare endocrine disorder derived from the defective activation of the cAMP pathway by the parathyroid hormone secondary to... 
Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Parathyroid hormone | Genetic aspects | brachydactyly-mental retardation syndrome | GNAS | pseudohypoparathyroidism | 2q37 deletion | Albright hereditary osteodystrophy
Journal Article
Biochemical and biophysical research communications, ISSN 0006-291X, 2002, Volume 296, Issue 1, pp. 67 - 72
Albright hereditary osteodystrophy (AHO) is characterized by multiple somatic defects secondary to mutations in the GNAS1 gene. AHO patients with mutations on... 
GNAS1 | Imprinting | Pseudohypoparathyroidism | Genetics | G proteins | Hormones | Albright hereditary osteodystrophy
Journal Article
Current opinion in endocrinology, diabetes, and obesity, ISSN 1752-296X, 11/2016, Volume 24, Issue 1, pp. 1 - 38
Purpose of review To provide readers with a review of contemporary literature describing the evolving understanding of the pseudohypoparathyroidism type 1A... 
GNAS | Albright Hereditary Osteodystrophy | Hormone resistance | Pseudohypoparathyroidism | Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Index Medicus
Journal Article
Hormone and metabolic research, ISSN 0018-5043, 11/2014, Volume 46, Issue 12, pp. 841 - 844
Abstract GNAS is a complex imprinted locus with multiple oppositely imprinted gene products, including the G protein α-subunit G s α that is expressed... 
Review | pseudohypoparathyroidism | genomic imprinting | Albright hereditary osteodystrophy | obesity
Journal Article
Current opinion in endocrinology, diabetes, and obesity, ISSN 1752-296X, 2/2017, Volume 24, Issue 1, pp. 33 - 38
Journal Article
Medicine (Baltimore), ISSN 0025-7974, 05/2020, Volume 99, Issue 21, pp. e19965 - e19965
Introduction: Pseudohypoparathyroidism (PHP) indicates a group of rare disorders characterized by end-organ resistance to various hormones, primarily... 
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Medical colleges | Vitamin D | Parathyroid hormone | Calcium carbonate | Genetic research | Calcifediol | Glycoproteins | Genetic aspects | Alfacalcidol | Mental illness | Index Medicus | Abridged Index Medicus
Journal Article
Journal Article
Annals of dermatology, ISSN 1013-9087, 2009, Volume 21, Issue 2, pp. 154 - 158
Primary osteoma cutis is characterized by the formation of normal bone tissue in the dermis or subcutis without any underlying tissue abnormality or... 
Pseudopseudohypoparathyroidism | Albright hereditary osteodystrophy | Osteoma cutis | Pseudohypoparathyroidism | Life Sciences & Biomedicine | Dermatology | Science & Technology | Case Report | 피부과학
Journal Article