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/vufind/Search/Results?lookfor=%22Lahiry%2C+Piya%22&type=Person&sort=year
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PubPharm (27)
1
Late preterm birth and growth trajectories during childhood : a linked retrospective cohort study
enthalten in:
BMC pediatrics
| 2023
von
Yoshida-Montezuma, Y.
|
Kirkwood, D.
|
Sivapathasundaram, B.
| +109
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2
Choosing Wisely : The Canadian Rheumatology Association Pediatric Committee's List of Items Physicians and Patients Should Question
enthalten in:
The Journal of rheumatology
| 2023
von
Lim, L.
|
McMillan, T.
|
Chédeville, G.
| +12
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3
Hemophagocytic Lymphohistiocytosis Gene Variants in Childhood-Onset Systemic Lupus Erythematosus With Macrophage Activation Syndrome
enthalten in:
The Journal of rheumatology
| 2022
von
Lahiry, P.
|
Naumenko, S.
|
Couse, M.
| +7
CommentIn: J Rheumatol. 2022 Oct;49(10):1082-1084. - PMID 36271722
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4
Variations in Pediatric Rheumatology Workforce and Care Processes Across Canada
enthalten in:
The Journal of rheumatology
| 2022
von
Lee, J.
|
Laxer, R.
|
Feldman, B.
| +86
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5
A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome
enthalten in:
Cilia
| 2016
von
Oud, M.
|
Bonnard, C.
|
Mans, D.
| +18
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6
A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome
enthalten in:
Cilia
| 2016
von
Oud, M.
|
Bonnard, C.
|
Mans, D.
| +18
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7
A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome
enthalten in:
Cilia
| 2016
von
Oud, M.
|
Bonnard, C.
|
Mans, D.
| +18
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8
Exome sequencing identifies NFS1 deficiency in a novel Fe-S cluster disease, infantile mitochondrial complex II/III deficiency
enthalten in:
Molecular genetics & genomic medicine
| 2014
von
Farhan, S.
|
Wang, J.
|
Robinson, J.
| +7
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9
A mutation in the serine protease TMPRSS4 in a novel pediatric neurodegenerative disorder
enthalten in:
Orphanet journal of rare diseases
| 2013
von
Lahiry, P.
|
Racacho, L.
|
Wang, J.
| +6
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10
A mutation in the serine protease TMPRSS4 in a novel pediatric neurodegenerative disorder
enthalten in:
Orphanet journal of rare diseases
| 2013
von
Lahiry, P.
|
Racacho, L.
|
Wang, J.
| +6
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American journal of human genetics
3
Cilia
3
Current diabetes reports
3
The Journal of rheumatology
2
Journal of lipid research
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Journal of nutrigenetics and nutrigenomics
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Orphanet journal of rare diseases
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International journal of circumpolar health
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Methods in molecular biology (Clifton, N.J.)
1
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1
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1
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1
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Research Support, Non-U.S. Gov't
5
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3
Ciliary defects
3
Ciliopathy
3
ECO
3
Endocrine-cerebro-osteodysplasia syndrome
3
ICK
3
Intestinal cell kinase
3
SRTD
3
Short-rib thoracic dysplasia syndrome
2
Apolipoproteins A
2
Cholesterol Education Program Adult Treatment
2
Education Program Adult Treatment Panel
2
Metabolic Syndrome
2
National Cholesterol Education Program
2
Pro12Ala Polymorphism
1
1069-03-0
1
1750-12-5
1
2-keto-3-deoxyoctonate
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2010-2019
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2000-2009
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