Shovlin CL - Search Results

1

Comment on Kilian et al. Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT. J. Clin. Med. 2023, 12, 2704.

Eker OF, Dupuis-Girod S, Shovlin CL, Boccardi E. Eker OF, et al. Among authors: shovlin cl. J Clin Med. 2023 Nov 20;12(22):7179. doi: 10.3390/jcm12227179. J Clin Med. 2023. PMID: 38002793 Free PMC article.

2

Top dietary iron sources in the UK.

Finnamore HE, Whelan K, Hickson M, Shovlin CL. Finnamore HE, et al. Among authors: shovlin cl. Br J Gen Pract. 2014 Apr;64(621):172-3. doi: 10.3399/bjgp14X677761. Br J Gen Pract. 2014. PMID: 24686867 Free PMC article. No abstract available.

3

Low Dose Iron Treatments Induce a DNA Damage Response in Human Endothelial Cells within Minutes.

Mollet IG, Patel D, Govani FS, Giess A, Paschalaki K, Periyasamy M, Lidington EC, Mason JC, Jones MD, Game L, Ali S, Shovlin CL. Mollet IG, et al. Among authors: shovlin cl. PLoS One. 2016 Feb 11;11(2):e0147990. doi: 10.1371/journal.pone.0147990. eCollection 2016. PLoS One. 2016. PMID: 26866805 Free PMC article.

4

Low grade mosaicism in hereditary haemorrhagic telangiectasia identified by bidirectional whole genome sequencing reads through the 100,000 Genomes Project clinical diagnostic pipeline.

Clarke JM, Alikian M, Xiao S, Kasperaviciute D, Thomas E, Turbin I, Olupona K, Cifra E, Curetean E, Ferguson T, Redhead J; Genomics England Research Consortium; Shovlin CL. Clarke JM, et al. Among authors: shovlin cl. J Med Genet. 2020 Dec;57(12):859-862. doi: 10.1136/jmedgenet-2019-106794. Epub 2020 Apr 17. J Med Genet. 2020. PMID: 32303606 Free PMC article. No abstract available.

5

Adenosine deaminase deficiency with altered biochemical parameters in two sisters with late-onset immunodeficiency.

Fairbanks LD, Shovlin CL, Webster AD, Hughes JM, Simmonds HA. Fairbanks LD, et al. Among authors: shovlin cl. J Inherit Metab Dis. 1994;17(1):135-7. doi: 10.1007/BF00735418. J Inherit Metab Dis. 1994. PMID: 7914248 No abstract available.

6

Analysis of several endoglin mutants reveals no endogenous mature or secreted protein capable of interfering with normal endoglin function.

Paquet ME, Pece-Barbara N, Vera S, Cymerman U, Karabegovic A, Shovlin C, Letarte M. Paquet ME, et al. Hum Mol Genet. 2001 Jun 15;10(13):1347-57. doi: 10.1093/hmg/10.13.1347. Hum Mol Genet. 2001. PMID: 11440987

7

Characterization of endoglin and identification of novel mutations in hereditary hemorrhagic telangiectasia.

Shovlin CL, Hughes JM, Scott J, Seidman CE, Seidman JG. Shovlin CL, et al. Am J Hum Genet. 1997 Jul;61(1):68-79. doi: 10.1086/513906. Am J Hum Genet. 1997. PMID: 9245986 Free PMC article.

8

Adenosine deaminase (ADA) deficiency as the unexpected cause of CD4+ T-lymphocytopenia in two HIV-negative adult female siblings.

Fairbanks LD, Simmonds HA, Webster AD, Shovlin CL, Hughes JM. Fairbanks LD, et al. Among authors: shovlin cl. Adv Exp Med Biol. 1994;370:471-4. doi: 10.1007/978-1-4615-2584-4_100. Adv Exp Med Biol. 1994. PMID: 7660952 No abstract available.

9

Adult onset immunodeficiency caused by inherited adenosine deaminase deficiency.

Shovlin CL, Simmonds HA, Fairbanks LD, Deacock SJ, Hughes JM, Lechler RI, Webster AD, Sun XM, Webb JC, Soutar AK. Shovlin CL, et al. J Immunol. 1994 Sep 1;153(5):2331-9. J Immunol. 1994. PMID: 8051429

10

Genetic analysis of susceptibility to experimental autoimmune encephalomyelitis in a cross between SJL/J and B10.S mice.

Encinas JA, Lees MB, Sobel RA, Symonowicz C, Greer JM, Shovlin CL, Weiner HL, Seidman CE, Seidman JG, Kuchroo VK. Encinas JA, et al. Among authors: shovlin cl. J Immunol. 1996 Sep 1;157(5):2186-92. J Immunol. 1996. PMID: 8757345

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