Suchergebnisse - "Grant, Christina"

PubPharm (50)

1

De novovariants in the non-coding spliceosomal snRNA geneRNU4-2are a frequent cause of syndromic neurodevelopmental disorders

enthalten in: bioRxiv.org | 2024

von Chen, Y. | Dawes, R. | Kim, H. | +94

2

De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders

enthalten in: medRxiv : the preprint server for health sciences | 2024

von Chen, Y. | Dawes, R. | Kim, H. | +94

3

Mucopolysaccharidosis type VII (Sly syndrome) - What do we know?

enthalten in: Molecular genetics and metabolism | 2024

von Grant, C. | López-Valdez, J. | Marsden, D. | +1

4

Serious and life-threatening events associated with non-medical cannabis use in Canadian children and youth

enthalten in: Paediatrics & child health | 2024

von Grant, C. | Plebon-Huff, S. | Perwaiz, S. | +2

5

Implementation of a tier system for IVIG indications to address IVIG shortage at a tertiary care pediatric medical center

enthalten in: Pediatric blood & cancer | 2024

von Roth, K. | Darwish, C. | Keller, M. | +12

6

An updated management approach of Pompe disease patients with high-sustained anti-rhGAA IgG antibody titers : experience with bortezomib-based immunomodulation

enthalten in: Frontiers in immunology | 2024

von Desai, A. | Shrivastava, G. | Grant, C. | +3

7

Implementation of a tier system for IVIG indications to address IVIG shortage at a tertiary care pediatric medical center

enthalten in: Pediatric Blood & Cancer | 2024

von Roth, K. | Darwish, C. | Keller, M. | +12

8

Assessing the feasibility of an intervention for adolescents and parents transitioning out of paediatric eating disorder services : A mixed methods study

enthalten in: European eating disorders review : the journal of the Eating Disorders Association | 2023

von Nicula, M. | Kimber, M. | Boylan, K. | +7

9

Opportunities and challenges in capturing severe vaping-related injuries among Canadian children and youth

enthalten in: Preventive medicine reports | 2023

von Chadi, N. | Richmond, S. | Tulloch, T. | +3

10

De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities

enthalten in: NPJ genomic medicine | 2021

von Okur, V. | Chen, Z. | Vossaert, L. | +35

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