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Pediatric Radiology
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November 2, 2020
Genetics for paediatric radiologists
Schaida Schirwani, Jennifer Campbell
Clinical Dysmorphology
|
December 15, 2017
Clinical and molecular characterization of the first familial report of 1p32 microdeletion
Schaida Schirwani, Kath Smith, Meena Balasubramanian
Cureus
|
March 22, 2021
The Imbalance in Medico-Legal Cover Awareness and Uptake Between Overseas Junior Doctors and Local Graduates in the NHS
Mustafa Jalal, Schaida Schirwani, Karna Dev Bardhan
European Journal of Medical Genetics
|
February 27, 2025
Early onset basal cell carcinoma: Consider Bazex-Dupré-Christol syndrome
Aislinn Cragg, David Hunt, Hywel Cooper, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine
|
October 11, 2017
Carbamazepine Improves Apneic Episodes in Congenital Central Hypoventilation Syndrome (CCHS) With a Novel <i>PHOX2B</i> Exon 1 Missense Mutation
Schaida Schirwani, Karen Pysden, Philip Chetcuti, et al.
American Journal of Medical Genetics. Part A
|
April 23, 2018
Expanding the molecular basis and phenotypic spectrum of ZDHHC9-associated X-linked intellectual disability
Schaida Schirwani, Emma Wakeling, Kath Smith, et al.
Gene
|
November 6, 2018
Exploring the association between SRPX2 variants and neurodevelopment: How causal is it?
Schaida Schirwani, Vivienne McConnell, Josh Willoughby, et al.
The American Journal of Dermatopathology
|
January 3, 2024
Mosaic Muir Torre Syndrome: Keratoacanthoma as a Piece of the Puzzle
Amber O'Brien, Sarah Macfarlane, Matthew Sommerlad, et al.
The American Journal of Dermatopathology
|
June 24, 2025
Atypical Spitz Tumor (Spitz Melanocytoma) With Lymph Node Metastasis and Long-Term Clinical Follow-Up
Schaida Schirwani, Jeff Theaker, Lucy Side, et al.
Cancer Genetics
|
December 20, 2025
Multiple endocrine neoplasia type 1 syndrome due to novel Alu insertion
Aislinn Cragg, Hannah Boon, Treena Cranston, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
Pediatric Radiology
|
November 2, 2020
Genetics for paediatric radiologists
Schaida Schirwani, Jennifer Campbell
Clinical Dysmorphology
|
December 15, 2017
Clinical and molecular characterization of the first familial report of 1p32 microdeletion
Schaida Schirwani, Kath Smith, Meena Balasubramanian
Cureus
|
March 22, 2021
The Imbalance in Medico-Legal Cover Awareness and Uptake Between Overseas Junior Doctors and Local Graduates in the NHS
Mustafa Jalal, Schaida Schirwani, Karna Dev Bardhan
European Journal of Medical Genetics
|
February 27, 2025
Early onset basal cell carcinoma: Consider Bazex-Dupré-Christol syndrome
Aislinn Cragg, David Hunt, Hywel Cooper, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine
|
October 11, 2017
Carbamazepine Improves Apneic Episodes in Congenital Central Hypoventilation Syndrome (CCHS) With a Novel <i>PHOX2B</i> Exon 1 Missense Mutation
Schaida Schirwani, Karen Pysden, Philip Chetcuti, et al.
American Journal of Medical Genetics. Part A
|
April 23, 2018
Expanding the molecular basis and phenotypic spectrum of ZDHHC9-associated X-linked intellectual disability
Schaida Schirwani, Emma Wakeling, Kath Smith, et al.
Gene
|
November 6, 2018
Exploring the association between SRPX2 variants and neurodevelopment: How causal is it?
Schaida Schirwani, Vivienne McConnell, Josh Willoughby, et al.
The American Journal of Dermatopathology
|
January 3, 2024
Mosaic Muir Torre Syndrome: Keratoacanthoma as a Piece of the Puzzle
Amber O'Brien, Sarah Macfarlane, Matthew Sommerlad, et al.
The American Journal of Dermatopathology
|
June 24, 2025
Atypical Spitz Tumor (Spitz Melanocytoma) With Lymph Node Metastasis and Long-Term Clinical Follow-Up
Schaida Schirwani, Jeff Theaker, Lucy Side, et al.
Cancer Genetics
|
December 20, 2025
Multiple endocrine neoplasia type 1 syndrome due to novel Alu insertion
Aislinn Cragg, Hannah Boon, Treena Cranston, et al.
Page
of 3