Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins) von Mosbah, H, Donadille, B, Vatier, C, Janmaat, S, Atlan, M, Badens, C, Barat, P, Béliard, S, Beltrand, J, Ben Yaou, R, Bismuth, E, Boccara, F, Cariou, B, Chaouat, M, Charriot, G, Christin-Maitre, S, De Kerdanet, M, Delemer, B, Disse, E, Dubois, N, Eymard, B, Fève, B, Lascols, O, Mathurin, P, Nobécourt, E, Poujol-Robert, A, Prevost, G, Richard, P, Sellam, J, Tauveron, I, Treboz, D, Vergès, B, Vermot-Desroches, V, Wahbi, K, Jéru, I, Vantyghem, M C, Vigouroux, C

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Impact of HIV Infection Status on Interpretation of Quantitative PCR for Detection of Pneumocystis jirovecii von Louis, M, Guitard, J, Jodar, M, Ancelle, T, Magne, D, Lascols, O, Hennequin, C

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Discordance between immunochemistry of mismatch repair proteins and molecular testing of microsatellite instability in colorectal cancer von Guyot D'Asnières De Salins, A., Tachon, G., Cohen, R., Karayan-Tapon, L., Junca, A., Frouin, E., Godet, J., Evrard, C., Randrian, V., Duval, A., Svrcek, M., Lascols, O., Vignot, S., Coulet, F., André, T., Fléjou, J.-F., Cervera, P., Tougeron, D.

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Nuclear envelope-related lipodystrophies von Guénantin, A.C., Briand, N., Bidault, G., Afonso, P., Béréziat, V., Vatier, C., Lascols, O., Caron-Debarle, M., Capeau, J., Vigouroux, C.

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Human lipodystrophies linked to mutations in A-type lamins and to HIV protease inhibitor therapy are both associated with prelamin A accumulation, oxidative stress and premature ce... von Caron, M, Auclair, M, Donadille, B, Béréziat, V, Guerci, B, Laville, M, Narbonne, H, Bodemer, C, Lascols, O, Capeau, J, Vigouroux, C

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One-year metreleptin improves insulin secretion in patients with diabetes linked to genetic lipodystrophic syndromes von Vatier, C., Fetita, S., Boudou, P., Tchankou, C., Deville, L., Riveline, JP, Young, J., Mathivon, L., Travert, F., Morin, D., Cahen, J., Lascols, O., Andreelli, F., Reznik, Y., Mongeois, E., Madelaine, I., Vantyghem, MC, Gautier, JF, Vigouroux, C.

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Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and management von Avila, M., Dyment, D.A., Sagen, J.V., St-Onge, J., Moog, U., Chung, B.H.Y., Mo, S., Mansour, S., Albanese, A., Garcia, S., Martin, D.O., Lopez, A.A., Claudi, T., König, R., White, S.M., Sawyer, S.L., Bernstein, J.A., Slattery, L., Jobling, R.K., Yoon, G., Curry, C.J., Merrer, M.L., Luyer, B.L., Héron, D., Mathieu-Dramard, M., Bitoun, P., Odent, S., Amiel, J., Kuentz, P., Thevenon, J., Laville, M., Reznik, Y., Fagour, C., Nunes, M.-L., Delesalle, D., Manouvrier, S., Lascols, O., Huet, F., Binquet, C., Faivre, L., Rivière, J.-B., Vigouroux, C., Njølstad, P.R., Innes, A.M., Thauvin-Robinet, C.

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Novel compound heterozygous ABCC2 variants in patients with Dubin‐Johnson syndrome and intrahepatic cholestasis of pregnancy von Huynh, M.‐T., Chrétien, Y., Grison, S., Delaunay, J.‐L., Lascols, O., Tran, C.T., Goria, O., Ramond, M.‐J., Barbu, V.

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Hypoglycaemia revealing heterozygous insulin receptor mutations von Preumont, V, Feincoeur, C, Lascols, O, Courtillot, C, Touraine, P, Maiter, D, Vigouroux, C

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Tumours with loss of MSH6 expression are MSI-H when screened with a pentaplex of five mononucleotide repeats von You, J-F, Buhard, O, Ligtenberg, M J L, Kets, C M, Niessen, R C, Hofstra, R M W, Wagner, A, Dinjens, W N M, Colas, C, Lascols, O, Collura, A, Flejou, J-F, Duval, A, Hamelin, R

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Fertility and Obstetrical Complications in Women with LMNA-Related Familial Partial Lipodystrophy von Vantyghem, M. C., Vincent-Desplanques, D., Defrance-Faivre, F., Capeau, J., Fermon, C., Valat, A. S., Lascols, O., Hecart, A. C., Pigny, P., Delemer, B., Vigouroux, C., Wemeau, J. L.

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A New Clinical Condition Linked to a Novel Mutation in Lamins A and C with Generalized Lipoatrophy, Insulin-Resistant Diabetes, Disseminated Leukomelanodermic Papules, Liver Steato... von Caux, F., Dubosclard, E., Lascols, O., Buendia, B., Chazouillères, O., Cohen, A., Courvalin, J.-C., Laroche, L., Capeau, J., Vigouroux, C., Christin-Maitre, S.

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Ten-year improvement of insulin resistance and growth with recombinant human insulin-like growth factor 1 in a patient with insulin receptor mutations resulting in leprechaunism von de Kerdanet, M, Caron-Debarle, M, Nivot, S, Gaillot, T, Lascols, O, Fremont, B, Bonaure, M, Gie, S, Massart, C, Capeau, J

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Corrigendum to “Ten-year improvement of insulin resistance and growth with recombinant human insulin-like growth factor 1 in a patient with insulin receptor mutations resulting in... von de Kerdanet, M, Caron-Debarle, M, Nivot, S, Gaillot, T, Lascols, O, Fremont, B, Bonnaure-Mallet, M, Gie, S, Massart, C, Capeau, J

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Patients with Familial Partial Lipodystrophy of the Dunnigan Type Due to a LMNA R482W Mutation Show Muscular and Cardiac Abnormalities von Vantyghem, M. C., Pigny, P., Maurage, C. A., Rouaix-Emery, N., Stojkovic, T., Cuisset, J. M., Millaire, A., Lascols, O., Vermersch, P., Wemeau, J. L., Capeau, J., Vigouroux, C.

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Efficacy of pioglitazone in familial partial lipodystrophy of the Dunnigan type: a case report von Moreau, F, Boullu-Sanchis, S, Vigouroux, C, Lucescu, C, Lascols, O, Sapin, R, Ruimy, D, Guerci, B, Pinget, M, Jeandidier, N

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Vascular placental abnormalities and newborn death in a pregnant diabetic woman with familial partial lipodystrophy type 3: A possible role for peroxisome proliferator-activated re... von Castell, A.L, Hiéronimus, S, Lascols, O, Fournier, T, Fénichel, P

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Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoat... von VIGOUROUX, Corinne, MAGRE, Jocelyne, GRIMALDI, André, PIQUEMAL, Régis, TOURAINE, Philippe, TREMBATH, Richard C, CAPEAU, Jacqueline, VANTYGHEM, Marie-Christine, BOURUT, Charlotte, LASCOLS, Olivier, SHACKLETON, Sue, LLOYD, David J, GUERCI, Bruno, PADOVA, Giuseppina, VALENSI, Paul

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Acquired Generalized Lipodystrophy: A New Cause of Anti-PD-1 Immune-Related Diabetes von Jehl, Alexandre, Cugnet-Anceau, Christine, Vigouroux, Corinne, Legeay, Anne L, Dalle, Stéphane, Harou, Olivier, Marchand, Lucien, Lascols, Olivier, Caussy, Cyrielle, Thivolet, Charles, Laville, Martine, Disse, Emmanuel

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Methylation tolerance due to an O6-methylguanine DNA methyltransferase (MGMT) field defect in the colonic mucosa: an initiating step in the development of mismatch repair-deficient... von Svrcek, Magali, Buhard, Olivier, Colas, Chrystelle, Coulet, Florence, Dumont, Sylvie, Massaoudi, Illiasse, Lamri, Amel, Hamelin, Richard, Cosnes, Jacques, Oliveira, Carla, Seruca, Raquel, Gaub, Marie-Pierre, Legrain, Michèle, Collura, Ada, Lascols, Olivier, Tiret, Emmanuel, Fléjou, Jean-François, Duval, Alex

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