Baylor University Medical Center Proceedings April 2014, Volume 27, Number 2 | страница 114

209. Park J, Munagala I, Xu H, Blankenship D, Maffucci P, Chaussabel D,
Banchereau J, Pascual V, Cunningham-Rundles C. Interferon signature
in the blood in inflammatory common variable immune deficiency. PLoS
One 2013;8(9):e74893.
210. Schmitt N, Bustamante J, Bourdery L, Bentebibel SE, Boisson-Dupuis S,
Hamlin F, Tran MV, Blankenship D, Pascual V, Savino DA, Banchereau J,
Casanova JL, Ueno H. IL-12 receptor β1 deficiency alters in vivo T follicular
helper cell response in humans. Blood 2013;121(17):3375–3385.
211. Schmitt N, Ueno H. Blood Tfh cells come with colors. Immunity
2013;39(4):629–630.
212. Schmitt N, Ueno H. Human T follicular helper cells: development and
subsets. Adv Exp Med Biol 2013;785:87–94.
213. Voo KS, Bover L, Harline ML, Vien LT, Facchinetti V, Arima K, Kwak
LW, Liu YJ. Antibodies targeting human OX40 expand effector T cells
and block inducible and natural regulatory T cell function. J Immunol
2013;191(7):3641–3650.
214. Yu CI, Becker C, Wang Y, Marches F, Helft J, Leboeuf M, Anguiano
E, Pourpe S, Goller K, Pascual V, Banchereau J, Merad M, Palucka
K. Human CD1c+ dendritic cells drive the differentiation of CD103+
CD8+ mucosal effector T cells via the cytokine TGF-β. Immunity
2013;38(4):818–830.
215. Zhang Z, Bao M, Lu N, Weng L, Yuan B, Liu YJ. The E3 ubiquitin ligase
TRIM21 negatively regulates the innate immune response to intracellular
double-stranded DNA. Nat Immunol 2013;14(2):172–178.
INTERNAL MEDICINE AND FAMILY MEDICINE
Note: Most family medicine and internal medicine articles are subclassified by
specialty, even if generalists were first authors or coauthors.
216. Abdul-Karim R, Ryan C, Rangel C, Emmett M. Levamisole-induced
vasculitis. Proc (Bayl Univ Med Cent) 2013;26(2):163–165.
217. Arroyo M, Fenves AZ, Emmett M. The calcium-alkali syndrome. Proc
(Bayl Univ Med Cent) 2013;26(2):179–181.
218. Benjamin MM, Gummelt KL, Zaki R, Afzal A, Sloan L, Shamim S.
Herpes simplex virus meningitis complicated by ascending paralysis.
Proc (Bayl Univ Med Cent) 2013;26(3):265–267.
219. George J, Graves R, Meador R Jr. Inguinal lymphadenopathy as the initial
presentation of sarcoidosis. Proc (Bayl Univ Med Cent) 2013;26(2):161–162.
220. Ha KY, Tyring SK. Vibrio vulnificus necrotizing fasciitis preceding herpes
zoster. Proc (Bayl Univ Med Cent) 2013;26(1):55–57.
221. Mantas AM, Wells J, Trotter J. Kayser-Fleischer rings of acute Wilson’s
disease. Proc (Bayl Univ Med Cent) 2013;26(2):166–167.
222. Patel T, Tietze D, Mehta AN. Amlodipine overdose. Proc (Bayl Univ Med
Cent) 2013;26(4):410–411.
223. Robinson SD, Cooper B, Leday TV. Copper deficiency (hypocupremia)
and pancytopenia late after gastric bypass surgery. Proc (Bayl Univ Med
Cent) 2013;26(4):382–386.
METABOLIC DISEASES
224. Bottiglieri T. Folate, vitamin B12, and S-adenosylmethionine. Psychiatr
Clin North Am 2013;36(1):1–13.
225. Butler LM, Arning E, Wang R, Bottiglieri T, Govindarajan S, Gao YT,
Yuan JM. Prediagnostic levels of serum one-carbon metabolites and
risk of hepatocellular carcinoma. Cancer Epidemiol Biomarkers Prev
2013;22(10):1884–1893.
226. Christensen KE, Deng L, Leung KY, Arning E, Bottiglieri T, Malysheva
OV, Caudill MA, Krupenko NI, Greene ND, Jerome-Majewska L,
MacKenzie RE, Rozen R. A novel mouse model for genetic variation in
10-formyltetrahydrofolate synthetase exhibits disturbed purine synthesis
with impacts on pregnancy and embryonic development. Hum Mol Genet
2013;22(18):3705–3719.
227. Dainese L, Monin ML, Demeret S, Brochier G, Froissart R, Spraul
A, Schiffmann R, Seilhean D, Mochel F. Abnormal glycogen in
astrocytes is sufficient to cause adult polyglucosan body disease. Gene
2013;515(2):376–379.
228. Fonseca VA, Lavery LA, Thethi TK, Daoud Y, DeSouza C, Ovalle F, Denham
DS, Bottiglieri T, Sheehan P Rosenstock J. Metanx in type 2 diabetes with
,
peripheral neuropathy: a randomized trial. Am J Med 2013;126(2):141–149.

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229. Forni S, Pearl PL, Gibson KM, Yu Y, Sweetman L. Quantitation of
gamma-hydroxybutyric acid in dried blood spots: feasibility assessment
for newborn screening of succinic semialdehyde dehydrogenase (SSADH)
deficiency. Mol Genet Metab 2013;109(3):255–259.
230. Forni S, Pearl PL, Gibson KM, Yu Y, Sweetman L. Response to Stove
and colleagues concerning newborn screening of succinic semialdehyde
dehydrogenase (SSADH) deficiency in dried blood spots. Mol Genet
Metab 2013;110(1–2):196.
231. Gauthier N, Wu JW, Wang SP, Allard P, Mamer OA, Sweetman L, Moser
AB, Kratz L, Alvarez F, Robitaille Y, Lépine F, Mitchell GA. A liver-specific
defect of Acyl-CoA degradation produces hyperammonemia, hypoglycemia
and a distinct hepatic Acyl-CoA pattern. PLoS One 2013;8(7):e60581.
232. Glier MB, Ngai YF, Sulistyoningrum DC, Aleliunas RE, Bottiglieri T,
Devlin AM. Tissue-specific relationship of S-adenosylhomocysteine
with allele-specific H19/Igf2 methylation and imprinting in mice with
hyperhomocysteinemia. Epigenetics 2013;8(1):44–53.
233. Inoue-Choi M, Nelson HH, Robien K, Arning E, Bottiglieri T, Koh WP,
Yuan JM. Plasma S-adenosylmethionine, DNMT polymorphisms, and
peripheral blood LINE-1 methylation among healthy Chinese adults in
Singapore. BMC Cancer 2013;13(1):389.
234. Lai SC, Nakayama Y, Sequeira JM, Wlodarczyk BJ, Cabrera RM, Finnell
RH, Bottiglieri T, Quadros EV. The transcobalamin receptor knockout
mouse: a model for vitamin B12 deficiency in the central nervous system.
FASEB J 2013;27(6):2468–2475.
235. Meng XL, Eto Y, Schiffmann R, Shen JS. HIV tat domain improves crosscorrection of human galactocerebrosidase in a gene- and flanking sequencedependent manner. Mol Ther Nucleic Acids 2013 Oct 22;2:e130.
236. Schiffmann R, Ries M, Blankenship D, Nicholls K, Mehta A, Clarke
JT, Steiner RD, Beck M, Barshop BA,