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Items: 20

1.

Very Early-Onset Inflammatory Manifestations of X-Linked Chronic Granulomatous Disease.

Labrosse R, Abou-Diab J, Blincoe A, Cros G, Luu TM, Deslandres C, Dirks M, Fazilleau L, Ovetchkine P, Teira P, LeDeist F, Fernandez I, Touzot F, Decaluwe H, Halac U, Haddad E.

Front Immunol. 2017 Sep 26;8:1167. doi: 10.3389/fimmu.2017.01167. eCollection 2017.

2.

Clinical features of cytotoxic CD8+ T-lymphocyte deficiency in chronic rhinosinusitis patients: a demographic and functional study.

Gabra N, Alromaih S, Endam LM, Brito RM, Larivière F, Al-Mot S, LeDeist F, Desrosiers M.

Int Forum Allergy Rhinol. 2014 Jun;4(6):495-501. doi: 10.1002/alr.21313. Epub 2014 Mar 17.

PMID:
24639246
3.

A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency.

Lee YN, Frugoni F, Dobbs K, Walter JE, Giliani S, Gennery AR, Al-Herz W, Haddad E, LeDeist F, Bleesing JH, Henderson LA, Pai SY, Nelson RP, El-Ghoneimy DH, El-Feky RA, Reda SM, Hossny E, Soler-Palacin P, Fuleihan RL, Patel NC, Massaad MJ, Geha RS, Puck JM, Palma P, Cancrini C, Chen K, Vihinen M, Alt FW, Notarangelo LD.

J Allergy Clin Immunol. 2014 Apr;133(4):1099-108. doi: 10.1016/j.jaci.2013.10.007. Epub 2013 Nov 28.

4.

ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia.

McCarl CA, Picard C, Khalil S, Kawasaki T, Röther J, Papolos A, Kutok J, Hivroz C, Ledeist F, Plogmann K, Ehl S, Notheis G, Albert MH, Belohradsky BH, Kirschner J, Rao A, Fischer A, Feske S.

J Allergy Clin Immunol. 2009 Dec;124(6):1311-1318.e7. doi: 10.1016/j.jaci.2009.10.007.

5.

STIM1 mutation associated with a syndrome of immunodeficiency and autoimmunity.

Picard C, McCarl CA, Papolos A, Khalil S, Lüthy K, Hivroz C, LeDeist F, Rieux-Laucat F, Rechavi G, Rao A, Fischer A, Feske S.

N Engl J Med. 2009 May 7;360(19):1971-80. doi: 10.1056/NEJMoa0900082.

6.

Rituximab therapy for childhood Evans syndrome.

Bader-Meunier B, Aladjidi N, Bellmann F, Monpoux F, Nelken B, Robert A, Armari-Alla C, Picard C, Ledeist F, Munzer M, Yacouben K, Bertrand Y, Pariente A, Chaussé A, Perel Y, Leverger G.

Haematologica. 2007 Dec;92(12):1691-4.

7.

[Auto-immune hemolytic anemia and dyserythropoïesis as the presenting signs of Fas-deficient condition in 3 children].

Guitton C, Ledeist F, Tchernia G, Bader-Meunier B.

Arch Pediatr. 2006 Apr;13(4):367-70. Epub 2006 Mar 9. French.

PMID:
16524705
8.

Dyserythropoiesis associated with a fas-deficient condition in childhood.

Bader-Meunier B, Rieux-Laucat F, Croisille L, Yvart J, Mielot F, Dommergues JP, Ledeist F, Tchernia G.

Br J Haematol. 2000 Feb;108(2):300-4.

PMID:
10691859
9.

A non-XLA primary deficiency causes the earliest known defect of B cell differentiation in humans: a comparison with an XLA case.

Meffre E, LeDeist F, de Saint-Basile G, Deville A, Fougereau M, Fischer A, Schiff C.

Immunol Lett. 1997 Jun 1;57(1-3):93-9.

PMID:
9232432
10.

A human non-XLA immunodeficiency disease characterized by blockage of B cell development at an early proB cell stage.

Meffre E, LeDeist F, de Saint-Basile G, Deville A, Fougereau M, Fischer A, Schiff C.

J Clin Invest. 1996 Oct 1;98(7):1519-26.

11.

Molecular cytogenetic analysis of a series of 23 DiGeorge syndrome patients by fluorescence in situ hybridization.

Demczuk S, Desmaze C, Aikem M, Prieur M, Ledeist F, Sanson M, Rouleau G, Thomas G, Aurias A.

Ann Genet. 1994;37(2):60-5.

PMID:
7985979
12.

Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases.

Desmaze C, Prieur M, Amblard F, Aikem M, LeDeist F, Demczuk S, Zucman J, Plougastel B, Delattre O, Croquette MF, et al.

Am J Hum Genet. 1993 Dec;53(6):1239-49.

13.

Major histocompatibility complex class II deficiency: clinical manifestations, immunologic features, and outcome.

Klein C, Lisowska-Grospierre B, LeDeist F, Fischer A, Griscelli C.

J Pediatr. 1993 Dec;123(6):921-8.

PMID:
8229525
14.

Treatment of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins, steroids, and cyclosporin A.

Stéphan JL, Donadieu J, Ledeist F, Blanche S, Griscelli C, Fischer A.

Blood. 1993 Oct 15;82(8):2319-23.

15.

An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome.

Jeanpierre M, Turleau C, Aurias A, Prieur M, Ledeist F, Fischer A, Viegas-Pequignot E.

Hum Mol Genet. 1993 Jun;2(6):731-5.

PMID:
8102570
16.

Unusual T cell clones in a patient with Nijmegen breakage syndrome.

Stoppa-Lyonnet D, Girault D, LeDeist F, Aurias A.

J Med Genet. 1992 Feb;29(2):136-7.

17.

Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.

Rötig A, Cormier V, Blanche S, Bonnefont JP, Ledeist F, Romero N, Schmitz J, Rustin P, Fischer A, Saudubray JM, et al.

J Clin Invest. 1990 Nov;86(5):1601-8.

18.

Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies.

Turleau C, Cabanis MO, Girault D, Ledeist F, Mettey R, Puissant H, Prieur M, de Grouchy J.

Am J Med Genet. 1989 Mar;32(3):420-4.

PMID:
2729362
19.

[Omenn's reticuloendotheliosis].

de Prost Y, Fischer A, Boccon-Gibod L, Larrègue M, Ledeist F, Mougenot JF, Griscelli C.

Ann Dermatol Venereol. 1983;110(9):763-4. French. No abstract available.

PMID:
6660785
20.

Heterogeneity of immunologic and enzymatic deficiencies in the familial reticuloendotheliosis syndrome.

Fischer A, Ledeist F, Durandy A, Hamet M, Arnaud-Battandier F, Griscelli C.

Birth Defects Orig Artic Ser. 1983;19(3):317-9. No abstract available.

PMID:
6317084

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