Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia von Bottomley, Sylvia S, Campagna, Dean R, Matsuoka, Makoto, Guernsey, Duane L, Rideout, Andrea, Dyack, Sarah, Samuels, Mark E, Kellogg, Mark D, Schmidt, Paul J, Nightingale, Mathew, Jiang, Haiyan, Ludman, Mark, Saint-Amant, Louis, Lachance, Mathieu, Ferguson, Meghan, Fernandez, Conrad V, Evans, Susan C, Fleming, Mark D, Orr, Andrew

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A novel syndrome of congenital sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay (SIFD) von Wiseman, Daniel H., May, Alison, Jolles, Stephen, Connor, Philip, Powell, Colin, Heeney, Matthew M., Giardina, Patricia J., Klaassen, Robert J., Chakraborty, Pranesh, Geraghty, Michael T., Major-Cook, Nathalie, Kannengiesser, Caroline, Thuret, Isabelle, Thompson, Alexis A., Marques, Laura, Hughes, Stephen, Bonney, Denise K., Bottomley, Sylvia S., Fleming, Mark D., Wynn, Robert F.

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A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemia von Lichtenstein, Daniel A., Crispin, Andrew W., Sendamarai, Anoop K., Campagna, Dean R., Schmitz-Abe, Klaus, Sousa, Cristovao M., Kafina, Martin D., Schmidt, Paul J., Niemeyer, Charlotte M., Porter, John, May, Alison, Patnaik, Mrinal M., Heeney, Matthew M., Kimmelman, Alec, Bottomley, Sylvia S., Paw, Barry H., Markianos, Kyriacos, Fleming, Mark D.

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Systematic molecular genetic analysis of congenital sideroblastic anemia: Evidence for genetic heterogeneity and identification of novel mutations von Bergmann, Anke K., Campagna, Dean R., McLoughlin, Erin M., Agarwal, Suneet, Fleming, Mark D., Bottomley, Sylvia S., Neufeld, Ellis J.

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Cost-effectiveness of routine imaging of suspected appendicitis von D'Souza, N, Marsden, M, Bottomley, S, Nagarajah, N, Scutt, F, Toh, S

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Recurrent heteroplasmy for the MT-ATP6 p.Ser148Asn (m.8969G>A) mutation in patients with syndromic congenital sideroblastic anemia of variable clinical severity von Berhe, Simon, Heeney, Matthew M, Campagna, Dean R, Thompson, John F, White, Eric J, Ross, Tristen, Peake, Roy Wa, Hanrahan, Jeffery D, Rodriguez, Vilmarie, Renaud, Deborah L, Patnaik, Mrinal S, Chang, Eugenia, Bottomley, Sylvia S, Fleming, Mark D

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CNS demyelination associated with copper deficiency and hyperzincemia von PRODAN, C. I, HOLLAND, N. R, WISDOM, P. J, BURSTEIN, S. A, BOTTOMLEY, S. S

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X‐linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA‐binding site mutations von Campagna, Dean R., Bie, Charlotte I., Schmitz‐Abe, Klaus, Sweeney, Marion, Sendamarai, Anoop K., Schmidt, Paul J., Heeney, Matthew M., Yntema, Helger G., Kannengiesser, Caroline, Grandchamp, Bernard, Niemeyer, Charlotte M., Knoers, Nine V.A.M., Swart, Sonia, Marron, Gordon, Wijk, Richard, Raymakers, Reinier A., May, Alison, Markianos, Kyriacos, Bottomley, Sylvia S., Swinkels, Dorine W., Fleming, Mark D.

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Bereavement in the Aftermath of Suicide, Overdose, and Sudden-Natural Death: Evaluating a New Measure of Needs von Bottomley, Jamison S., Smigelsky, Melissa A.

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Examining bereavement‐related needs and outcomes among survivors of sudden loss: A latent profile analysis von Bottomley, Jamison S., Campbell, Kevin W., Neimeyer, Robert A.

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A concurrent examination of protective factors associated with resilience and posttraumatic growth following childhood victimization von Schaefer, Lauren M., Howell, Kathryn H., Schwartz, Laura E., Bottomley, Jamison S., Crossnine, Candice B.

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Exploring the mental health correlates of overdose loss von Bottomley, Jamison S., Feigelman, William T., Rheingold, Alyssa A.

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Engineered bacterial lipoate protein ligase A (lplA) restores lipoylation in cell models of lipoylation deficiency von Bick, Nolan R., Dreishpoon, Margaret B., Perry, Ava, Rogachevskaya, Anna, Bottomley, Sylvia S., Fleming, Mark D., Ducamp, Sarah, Tsvetkov, Peter

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Domains of Social Support That Predict Bereavement Distress Following Homicide Loss: Assessing Need and Satisfaction von Bottomley, Jamison S., Burke, Laurie A., Neimeyer, Robert A.

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Dopamine promotes α‐synuclein aggregation into SDS‐resistant soluble oligomers via a distinct folding pathway von Cappai, Roberto, Leck, Su‐Ling, Tew, Deborah J., Williamson, Nicholas A., Smith, David P., Galatis, Denise, Sharpies, Robyn A., Curtain, Cyril C., Ali, Feda' E., Cherny, Robert A., Culvenor, Janetta G., Bottomley, Stephen P., Masters, Colin L., Barnham, Kevin J., Hill, Andrew F.

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Relapsing hypocupraemic myelopathy requiring high-dose oral copper replacement von Prodan, C I, Bottomley, S S, Holland, N R, Lind, S E

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Three novel mutations in ASIP associated with black fibre in alpacas (Vicugna pacos) von FEELEY, N. L., BOTTOMLEY, S., MUNYARD, K. A.

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Personality and Grief-Related Panic Attacks: Analysis of Neuroticism, Worry, and Anxiety Sensitivity von Lee, Sherman A., Bottomley, Jamison S.

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Predictors of Stigma, Guilt, and Shame among Adults Bereaved by Fatal Overdose von Bottomley, Jamison S., Campbell, Kevin W., Titlestad, Kristine B., Feigelman, William, Rheingold, Alyssa A.

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Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD) von Chakraborty, Pranesh K., Schmitz-Abe, Klaus, Kennedy, Erin K., Mamady, Hapsatou, Naas, Turaya, Durie, Danielle, Campagna, Dean R., Lau, Ashley, Sendamarai, Anoop K., Wiseman, Daniel H., May, Alison, Jolles, Stephen, Connor, Philip, Powell, Colin, Heeney, Matthew M., Giardina, Patricia-Jane, Klaassen, Robert J., Kannengiesser, Caroline, Thuret, Isabelle, Thompson, Alexis A., Marques, Laura, Hughes, Stephen, Bonney, Denise K., Bottomley, Sylvia S., Wynn, Robert F., Laxer, Ronald M., Minniti, Caterina P., Moppett, John, Bordon, Victoria, Geraghty, Michael, Joyce, Paul B.M., Markianos, Kyriacos, Rudner, Adam D., Holcik, Martin, Fleming, Mark D.

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