Omoyinmi, E.: search on Z-Library

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1

Efficacy and safety of anakinra for undifferentiated autoinflammatory diseases in children: a retrospective case review

Garg, Suchika, Wynne, Karen, Omoyinmi, Ebun, Eleftheriou, Despina, Brogan, Paul

Journal:

Rheumatology Advances in Practice

Year:

2019

Language:

english

File:

PDF, 116 KB

english, 2019

2

British kindred with dominant FMF associated with high incidence of AA amyloidosis caused by novel MEFV variant, and a review of the literature

Rowczenio, Dorota M, Youngstein, Taryn, Trojer, Hadija, Omoyinmi, Ebun, Baginska, Anna, Brogan, Paul, Papadopoulou, Charalampia, Rezk, Tamer, Hawkins, Philip N, Lachmann, Helen J

Journal:

Year:

2019

Language:

english

File:

PDF, 247 KB

english, 2019

3

Development and Validation of a Targeted Next-Generation Sequencing Gene Panel for Children With Neuroinflammation

McCreary, Dara, Omoyinmi, Ebun, Hong, Ying, Mulhern, Ciara, Papadopoulou, Charalampia, Casimir, Marina, Hacohen, Yael, Nyanhete, Rodney, Ahlfors, Helena, Cullup, Thomas, Lim, Ming, Gilmour, Kimberly,

Journal:

JAMA Network Open

Year:

2019

Language:

english

File:

PDF, 2.19 MB

english, 2019

4

SAT0010 A Targeted Next-Generation Sequencing Gene Panel for Autoinflammation

Omoyinmi, E., Standing, A., Keylock, A., Rowczenio, D., Melo Gomes, S., Cullup, T., Jenkins, L., Gilmour, K., Eleftheriou, D., Lachmann, H., Hawkins, P., Klein, N., Brogan, P.

Journal:

Annals of the Rheumatic Diseases

Year:

2016

Language:

english

File:

PDF, 65 KB

english, 2016

5

Inflammatory Arthritis as a Possible Feature of Coffin-Siris Syndrome

Melo Gomes, Sonia, Dias, Cristina, Omoyinmi, Ebun, Compeyrot-Lacassagne, Sandrine, Klein, Nigel, Sebire, Neil J., Brogan, Paul

Journal:

Year:

2019

Language:

english

File:

PDF, 1.04 MB

english, 2019

6

Deficiency of adenosine deaminase type 2 (DADA2): A description of phenotype and genotype in 15 cases

Nanthapisal, Sira, Murphy, Claire, Omoyinmi, Ebun, Hong, Ying, Standing, Ariane, Berg, Stefan, Ekelund, Maria, Jolles, Stephen, Harper, Lorraine, Youngstein, Taryn, Gilmour, Kimberly, Klein, Nigel, El

Journal:

Arthritis & Rheumatology

Year:

2016

Language:

english

File:

PDF, 898 KB

english, 2016

7

Extensive Oral Scarring and Bilateral Subclavian Artery Stenosis in Pediatric-Onset Behçet’s Disease

Vignesh, Pandiarajan, Singhal, Manphool, Suri, Deepti, Kakkar, Nandita, Omoyinmi, Ebun, Brogan, Paul, Singh, Surjit

Journal:

JCR Journal of Clinical Rheumatology

Year:

2018

File:

PDF, 263 KB

2018

8

Secondary C1q Deficiency in Activated PI3Kδ Syndrome Type 2

Hong, Ying, Nanthapisal, Sira, Omoyinmi, Ebun, Olbrich, Peter, Neth, Olaf, Speckmann, Carsten, Lucena, Jose Manuel, Gilmour, Kimberly, Worth, Austen, Klein, Nigel, Eleftheriou, Despina, Brogan, Paul

Journal:

Frontiers in Immunology

Year:

2019

File:

PDF, 606 KB

2019

9

Molecular genetic investigation, clinical features and response to treatment in 21 patients with Schnitzler's syndrome

Rowczenio, Dorota M., Pathak, Shelly, Arostegui, Juan I., Mensa-Vilaro, Anna, Omoyinmi, Ebun, Brogan, Paul, Lipsker, Dan, Scambler, Thomas, Owen, Roger, Trojer, Hadija, Baginska, Anna, Gillmore, Julia

Journal:

Year:

2017

Language:

english

File:

PDF, 798 KB

english, 2017

10

Monogenic polyarteritis nodosa caused by ADA2 Deficiency: the GOSH experience

Nanthapisal, S, Murphy, C, Omoyinmi, E, Standing, A, Hong, Y, Gomes, SM, Klein, N, Eleftheriou, D, Brogan, PA

Journal:

Pediatric Rheumatology

Year:

2015

Language:

english

File:

PDF, 226 KB

english, 2015

11

Testicular ischemia in deficiency of adenosine deaminase 2 (DADA2)

Clarke, Katherine, Campbell, Cathy, Omoyinmi, Ebun, Hong, Ying, Al Obaidi, Muthana, Sebire, Neil, Brogan, Paul A.

Journal:

Pediatric Rheumatology

Year:

2019

File:

PDF, 1.20 MB

2019

12

Late-Onset Cryopyrin-Associated Periodic Syndromes Caused by Somatic NLRP3 Mosaicism—UK Single Center Experience

Rowczenio, Dorota M., Gomes, Sónia Melo, Aróstegui, Juan I., Mensa-Vilaro, Anna, Omoyinmi, Ebun, Trojer, Hadija, Baginska, Anna, Baroja-Mazo, Alberto, Pelegrin, Pablo, Savic, Sinisa, Lane, Thirusha, W

Journal:

Frontiers in Immunology

Year:

2017

Language:

english

File:

PDF, 936 KB

english, 2017

13

PW02-031 - Genetic and clinical manifestations of CAPS

AK Bybee,H Lachmann,E Omoyinmi,B Nedjai,P Woo,T Lane…

Journal:

Pediatric Rheumatology

Year:

2013

Language:

english

File:

PDF, 99 KB

english, 2013

14

Autoinflammation due to homozygous S208 MEFV mutation

Hong, Ying, Standing, Ariane S I, Nanthapisal, Sira, Sebire, Neil, Jolles, Stephen, Omoyinmi, Ebun, Verstegen, Ruud HJ, Brogan, Paul A, Eleftheriou, Despina

Journal:

Annals of the Rheumatic Diseases

Year:

2018

Language:

english

File:

PDF, 463 KB

english, 2018

15

Stimulator of Interferon Genes-Associated Vasculitis of Infancy

Omoyinmi, Ebun, Melo Gomes, Sonia, Nanthapisal, Sira, Woo, Patricia, Standing, Ariane, Eleftheriou, Despina, Klein, Nigel, Brogan, Paul A.

Journal:

Arthritis & Rheumatology

Year:

2015

Language:

english

File:

PDF, 521 KB

english, 2015

16

Cutaneous Vasculitis and Digital Ischaemia Caused by Heterozygous Gain-of-Function Mutation in C3

Omoyinmi, Ebun, Mohamoud, Iman, Gilmour, Kimberly, Brogan, Paul A., Eleftheriou, Despina

Journal:

Frontiers in Immunology

Year:

2018

Language:

english

File:

PDF, 888 KB

english, 2018

17

Brief Report: Whole-Exome Sequencing Revealing Somatic NLRP3 Mosaicism in a Patient With Chronic Infantile Neurologic, Cutaneous, Articular Syndrome

Omoyinmi, Ebun, Melo Gomes, Sónia, Standing, Ariane, Rowczenio, Dorota M., Eleftheriou, Despina, Klein, Nigel, Aróstegui, Juan I., Lachmann, Helen J., Hawkins, Philip N., Brogan, Paul A.

Journal:

Arthritis & Rheumatology

Year:

2014

Language:

english

File:

PDF, 209 KB

english, 2014

18

Association of the IL-10 Gene Family Locus on Chromosome 1 with Juvenile Idiopathic Arthritis (JIA)

Omoyinmi, Ebun, Forabosco, Paola, Hamaoui, Raja, Bryant, Annette, Hinks, Anne, Ursu, Simona, Wedderburn, Lucy R., Thomson, Wendy, Lewis, Cathryn M., Woo, Patricia, Zirlik, Andreas

Journal:

Year:

2012

Language:

english

File:

PDF, 561 KB

english, 2012

19

A case of Myhre syndrome mimicking juvenile scleroderma

Jensen, Barbara, James, Rebecca, Hong, Ying, Omoyinmi, Ebun, Pilkington, Clarissa, Sebire, Neil J., Howell, Kevin J., Brogan, Paul A., Eleftheriou, Despina

Journal:

Pediatric Rheumatology

Year:

2020

File:

PDF, 844 KB

2020

20

Mitochondrial and oxidative stress genes are differentially expressed in neutrophils of sJIA patients treated with tocilizumab: a pilot microarray study

Omoyinmi, Ebun, Hamaoui, Raja, Bryant, Annette, Jiang, Mike Chao, Athigapanich, Trin, Eleftheriou, Despina, Hubank, Mike, Brogan, Paul, Woo, Patricia

Journal:

Pediatric Rheumatology

Year:

2016

Language:

english

File:

PDF, 1.31 MB

english, 2016

21

Late onset of the cryopyrin-associated periodic syndrome (CAPS) associated with low level of somatic mosaicism in six patients

Rowczenio, D, Gomes, S, Aróstegui, J, Omoyinmi, E, Gonzalez-Roca, E, Standing, A, Eleftheriou, D, Klein, N, Brogan, P, Lachmann, H, Hawkins, P

Journal:

Pediatric Rheumatology

Year:

2015

Language:

english

File:

PDF, 267 KB

english, 2015

22

Cutaneous Vasculitis and Recurrent Infection Caused by Deficiency in Complement Factor I

Nanthapisal, Sira, Eleftheriou, Despina, Gilmour, Kimberly, Leone, Valentina, Ramnath, Radhika, Omoyinmi, Ebun, Hong, Ying, Klein, Nigel, Brogan, Paul A.

Journal:

Frontiers in Immunology

Year:

2018

Language:

english

File:

PDF, 905 KB

english, 2018

23

[BMJ Publishing Group Ltd and European League Against Rheumatism Annual European Congress of Rheumatology, EULAR 2019, Madrid, 12â15 June 2019 - ()] Poster Presentations - FRI0001âNEXT GENERATION SEQUENCING ANALYSIS OF AN NLRP3 MUTATION NEGATIVE CAPS COHORT

Gomes, Sonia Melo, Omoyinmi, Ebun, Arostegui, Juan, Hong, Ying, Klein, Nigel, Brogan, Paul

Year:

2019

File:

PDF, 47 KB

2019

24

Gene hunting in autoinflammation

Standing, Ariane, Omoyinmi, Ebun, Brogan, Paul

Journal:

Clinical and Translational Allergy

Year:

2013

Language:

english

File:

PDF, 191 KB

english, 2013

25

Identification of a novel monogenic autoinflammatory disease due to mutation in a mitochondrial chaperone protein in a single kindred, and cure with allogeneic haematopoietic stem cell transplantation

Standing, Ariane, Paisan-Ruiz, Coro, Eleftheriou, Despina, Hong, Ying, Omoyinmi, Ebun, Rowcenzio, Dorota, Lachmann, Helen, Hawkins, Philip, Woo, Patricia, Klein, Nigel, Brogan, Paul

Journal:

Pediatric Rheumatology

Year:

2014

Language:

english

File:

PDF, 265 KB

english, 2014

26

Secondary C1q Deficiency in Activated PI3Kδ Syndrome Type 2

Hong, Ying, Nanthapisal, Sira, Omoyinmi, Ebun, Olbrich, Peter, Neth, Olaf, Speckmann, Carsten, Lucena, Jose Manuel, Gilmour, Kimberly, Worth, Austen, Klein, Nigel, Eleftheriou, Despina, Brogan, Paul

Journal:

Frontiers in Immunology

Year:

2019

Language:

english

File:

PDF, 606 KB

english, 2019

27

Extensive Oral Scarring and Bilateral Subclavian Artery Stenosis in Pediatric-Onset Behçet’s Disease

Vignesh, Pandiarajan, Singhal, Manphool, Suri, Deepti, Kakkar, Nandita, Omoyinmi, Ebun, Brogan, Paul, Singh, Surjit

Journal:

JCR Journal of Clinical Rheumatology

Year:

2018

File:

PDF, 263 KB

2018

28

TNF Receptor Associated Periodic Syndrome associated with gonosomal mosaicism of a novel 24 nucleotide TNFRSF1A deletion

Rowczenio, Dorota M., Trojer, Hadija, Omoyinmi, Ebun, Aróstegui, Juan I., Arakelov, Grigor, Mensa-Vilaro, Anna, Baginska, Anna, Pilorz, Caroline Silva, Wang, Guosu, Lane, Thirusha, Brogan, Paul, Hawki

Journal:

Arthritis & Rheumatology

Year:

2016

Language:

english

File:

PDF, 960 KB

english, 2016

29

Moyamoya-like cerebrovascular disease in a child with a novel mutation in myosin heavy chain 11

Keylock, Annette, Hong, Ying, Saunders, Dawn, Omoyinmi, Ebun, Mulhern, Ciara, Roebuck, Derek, Brogan, Paul, Ganesan, Vijeya, Eleftheriou, Despina

Journal:

Year:

2017

Language:

english

File:

PDF, 216 KB

english, 2017

30

De Novo PTEN Mutation in a Young Boy with Cutaneous Vasculitis

Mauro, Angela, Omoyinmi, Ebun, Sebire, Neil James, Barnicoat, Angela, Brogan, Paul

Journal:

Case Reports in Pediatrics

Year:

2017

Language:

english

File:

PDF, 1.63 MB

english, 2017

31

Janus kinase 1/2 inhibition for the treatment of autoinflammation associated with heterozygous TNFAIP3 mutation

Mulhern, Ciara M., Hong, Ying, Omoyinmi, Ebun, Jacques, Thomas S., D'Arco, Felice, Hemingway, Cheryl, Brogan, Paul A., Eleftheriou, Despina

Journal:

Journal of Allergy and Clinical Immunology

Year:

2019

Language:

english

File:

PDF, 1.15 MB

english, 2019

32

Autoinflammatory periodic fever, immunodeficiency, and thrombocytopenia (PFIT) caused by mutation in actin-regulatory gene WDR1

Standing, Ariane S.I., Malinova, Dessislava, Hong, Ying, Record, Julien, Moulding, Dale, Blundell, Michael P., Nowak, Karolin, Jones, Hannah, Omoyinmi, Ebun, Gilmour, Kimberly C., Medlar, Alan, Stanes

Journal:

Journal of Experimental Medicine

Year:

2017

Language:

english

File:

PDF, 2.12 MB

english, 2017

33

Cerebral arteriopathy associated with heterozygous variants in the casitas B-lineage lymphoma gene

Hong, Ying, Keylock, Annette, Jensen, Barbara, Jacques, Thomas S., Ogunbiyi, Olumide, Omoyinmi, Ebun, Saunders, Dawn, Mallick, Andrew A., Tooley, Madeleine, Newbury-Ecob, Ruth, Rankin, Julia, Williams

Journal:

Neurology: Genetics

Year:

2020

File:

PDF, 913 KB

2020

34

Th1 and Th17 cell subpopulations are enriched in the peripheral blood of patients with systemic juvenile idiopathic arthritis

Omoyinmi, E., Hamaoui, R., Pesenacker, A., Nistala, K., Moncrieffe, H., Ursu, S., Wedderburn, L. R., Woo, P.

Journal:

Year:

2012

Language:

english

File:

PDF, 219 KB

english, 2012

35

Early-Onset Juvenile SLE Associated With a Novel Mutation in Protein Kinase C δ

Nanthapisal, Sira, Omoyinmi, Ebun, Murphy, Claire, Standing, Ariane, Eisenhut, Michael, Eleftheriou, Despina, Brogan, Paul A.

Journal:

Year:

2017

Language:

english

File:

PDF, 951 KB

english, 2017

36

Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome: a report of a novel mutation and review of the literature

Kluk, J., Rustin, M., Brogan, P.A., Omoyinmi, E., Rowczenio, D.M., Willcocks, L.C., Melly, L., Lachmann, H.J.

Journal:

British Journal of Dermatology

Year:

2014

Language:

english

File:

PDF, 348 KB

english, 2014

37

Whole Exome Sequencing reveals a NLRP3 mutation in exon 5 in a patient with CINCA

Gomes, S, Arostegui, J, Omoyinmi, E, Standing, A, Klein, N, Lachmann, H, Hawkins, P, Brogan, P

Journal:

Pediatric Rheumatology

Year:

2015

Language:

english

File:

PDF, 267 KB

english, 2015

38

Testicular ischemia in deficiency of adenosine deaminase 2 (DADA2)

Clarke, Katherine, Campbell, Cathy, Omoyinmi, Ebun, Hong, Ying, Al Obaidi, Muthana, Sebire, Neil, Brogan, Paul A.

Journal:

Pediatric Rheumatology

Year:

2019

Language:

english

File:

PDF, 1.20 MB

english, 2019

39

Janus kinase inhibition for autoinflammation in DNASE2 deficiency

Hong, Ying, Capitani, Melania, Murphy, Claire, Pandey, Sumeet, Cavounidis, Athena, Takeshita, Haruo, Nanthapisal, Sira, Yasuda, Toshihiro, Bader-Meunier, Brigitte, McCreary, Dara, Omoyinmi, Ebun, Rao,

Journal:

Journal of Allergy and Clinical Immunology

Year:

2019

File:

PDF, 1.88 MB

2019

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