Glenda J. Sobey: search on Z-Library

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1

Ehlers–Danlos syndrome: how to diagnose and when to perform genetic tests

Journal:

Archives of Disease in Childhood

Year:

2015

Language:

english

File:

PDF, 593 KB

english, 2015

2

Ehlers-Danlos syndromes

Ghali, Neeti, Sobey, Glenda, Burrows, Nigel

Journal:

Year:

2019

Language:

english

File:

PDF, 1.98 MB

english, 2019

3

Arterial complications in classical Ehlers-Danlos syndrome: a case series

Angwin, Chloe, Brady, Angela F, Pope, F Michael, Vandersteen, Anthony, Baker, Duncan, Cheema, Harveer, Sobey, Glenda, Johnson, Diana, von Klemperer, Kate, Kazkaz, Hanadi, van Dijk, Fleur, Ghali, Neeti

Journal:

Journal of Medical Genetics

Year:

2020

File:

PDF, 812 KB

2020

4

Ehlers–Danlos syndrome: an update on classification by genotype and phenotypeI01. Classical and Vascular Ehlers–Danlos Syndrome: Characteristic Phenotypes and Genetic Markers

Journal:

Year:

2017

Language:

english

File:

PDF, 100 KB

english, 2017

5

Ehlers-Danlos syndrome, classical type

Bowen, Jessica M., Sobey, Glenda J., Burrows, Nigel P., Colombi, Marina, Lavallee, Mark E., Malfait, Fransiska, Francomano, Clair A.

Journal:

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Year:

2017

Language:

english

File:

PDF, 420 KB

english, 2017

6

A novel homozygous keratin 10 mutation in siblings with autosomal recessive epidermolytic ichthyosis

Balasubramanian, Meena, Terron-Kwiatkowski, Ana, Shah, Manu, Wagner, Bart E, Mechan, Dot, Baty, David, Sobey, Glenda J

Journal:

Expert Review of Dermatology

Year:

2010

Language:

english

File:

PDF, 1.62 MB

english, 2010

7

Prospective clinical investigations of children with periodontal EhlersâDanlos syndrome identify generalized lack of attached gingiva as a pathognomonic feature

Kapferer-Seebacher, Ines, Oakley-Hannibal, Elizabeth, Lepperdinger, Ulrike, Johnson, Diana, Ghali, Neeti, Brady, Angela F., Sobey, Glenda, Zschocke, Johannes, van Dijk, Fleur S.

Journal:

Genetics in Medicine

Year:

2020

File:

PDF, 883 KB

2020

8

Authorsâ reply to Mahmood, Borumandi, and Williams

Ghali, Neeti, Sobey, Glenda, Burrows, Nigel

Journal:

Year:

2019

File:

PDF, 690 KB

2019

9

Dermatosparaxis (Ehlers-Danlos Type VIIC): Prenatal Diagnosis Following a Previous Pregnancy With Unexpected Skull Fractures at Delivery

Solomons, Joyce, Coucke, Paul, Symoens, Sofie, Cohen, Marta C., Pope, F. Michael, Wagner, Bart E., Sobey, Glenda, Black, Rebecca, Cilliers, Deirdre

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 1.22 MB

english, 2013

10

Ehlers–Danlos syndrome: an update on classification by genotype and phenotypeI01. Classical and Vascular Ehlers–Danlos Syndrome: Characteristic Phenotypes and Genetic Markers

Journal:

Year:

2017

Language:

english

File:

PDF, 65 KB

english, 2017

11

DSE associated musculocontractural EDS, a milder phenotype or phenotypic variability

Schirwani, Schaida, Metcalfe, Kay, Wagner, Bart, Berry, Ian, Sobey, Glenda, Jewell, Rosalyn

Journal:

European Journal of Medical Genetics

Year:

2019

Language:

english

File:

PDF, 8.18 MB

english, 2019

12

Pattern of admissions to a tertiary dermatology unit in South Africa

Sue Jessop, Rowena McKenzie, James Milne, Solveig Rapp, Glenda Sobey

Journal:

International Journal of Dermatology

Year:

2002

Language:

english

File:

PDF, 101 KB

english, 2002

13

Mosaic Chromosome 6 Trisomy in an Epidermal Nevus

Glenda J. Sobey, Oliver W. Quarrell, Steven Williams, Helen M. McGrath

Journal:

Pediatric Dermatology

Year:

2007

Language:

english

File:

PDF, 506 KB

english, 2007

14

De Barsy syndrome: a review of the phenotype

Kivuva, Emma C., Parker, Michael J., Cohen, Marta C., Wagner, Bart E., Sobey, Glenda

Journal:

Clinical Dysmorphology

Year:

2008

Language:

english

File:

PDF, 322 KB

english, 2008

15

ESSENTIALS: EXPERTS IN THE FIELDI71. EHLERS–DANLOS AND COLLAGEN VASCULAR DISORDERS

Journal:

Year:

2017

Language:

english

File:

PDF, 27 KB

english, 2017

16

Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations

Pollitt, Rebecca C., Saraff, Vrinda, Dalton, Ann, Webb, Emma A., Shaw, Nick J., Sobey, Glenda J., Mughal, M. Zulf, Hobson, Emma, Ali, Farhan, Bishop, Nicholas J., Arundel, Paul, Högler, Wolfgang, Bala

Journal:

American Journal of Medical Genetics Part A

Year:

2016

Language:

english

File:

PDF, 433 KB

english, 2016

17

Ultrastructural and histological findings on examination of skin in osteogenesis imperfecta

Balasubramanian, Meena, Wagner, Bart E., Peres, Luiz C., Sobey, Glenda J., Parker, Michael J., Dalton, Ann, Arundel, Paul, Bishop, Nicholas J.

Journal:

Clinical Dysmorphology

Year:

2015

Language:

english

File:

PDF, 918 KB

english, 2015

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