Quartier P - Search Results

1

Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiency.

Hauck F, Randriamampita C, Martin E, Gerart S, Lambert N, Lim A, Soulier J, Maciorowski Z, Touzot F, Moshous D, Quartier P, Heritier S, Blanche S, Rieux-Laucat F, Brousse N, Callebaut I, Veillette A, Hivroz C, Fischer A, Latour S, Picard C. Hauck F, et al. Among authors: quartier p. J Allergy Clin Immunol. 2012 Nov;130(5):1144-1152.e11. doi: 10.1016/j.jaci.2012.07.029. Epub 2012 Sep 15. J Allergy Clin Immunol. 2012. PMID: 22985903

2

Germ-line transcription and methylation status of the TCR-J alpha locus in its accessible configuration.

Villey I, Quartier P, Selz F, de Villartay JP. Villey I, et al. Among authors: quartier p. Eur J Immunol. 1997 Jul;27(7):1619-25. doi: 10.1002/eji.1830270705. Eur J Immunol. 1997. PMID: 9247569

3

Early and prolonged intravenous immunoglobulin replacement therapy in childhood agammaglobulinemia: a retrospective survey of 31 patients.

Quartier P, Debré M, De Blic J, de Sauverzac R, Sayegh N, Jabado N, Haddad E, Blanche S, Casanova JL, Smith CI, Le Deist F, de Saint Basile G, Fischer A. Quartier P, et al. J Pediatr. 1999 May;134(5):589-96. doi: 10.1016/s0022-3476(99)70246-5. J Pediatr. 1999. PMID: 10228295

4

[Lymphomas in children infected with HIV-1].

Gandemer V, Verkarre V, Quartier P, Brousse N, Blanche S. Gandemer V, et al. Among authors: quartier p. Arch Pediatr. 2000 Jul;7(7):738-44. doi: 10.1016/s0929-693x(00)80154-2. Arch Pediatr. 2000. PMID: 10941489 French.

5

Enteroviral meningoencephalitis in X-linked agammaglobulinemia: intensive immunoglobulin therapy and sequential viral detection in cerebrospinal fluid by polymerase chain reaction.

Quartier P, Foray S, Casanova JL, Hau-Rainsard I, Blanche S, Fischer A. Quartier P, et al. Pediatr Infect Dis J. 2000 Nov;19(11):1106-8. doi: 10.1097/00006454-200011000-00020. Pediatr Infect Dis J. 2000. PMID: 11099099 No abstract available.

6

[IgA deficiency].

Quartier P. Quartier P. Arch Pediatr. 2001 Jun;8(6):629-33. doi: 10.1016/s0929-693x(00)00288-8. Arch Pediatr. 2001. PMID: 11446186 Review. French.

7

Propionibacterium acnes chest infections in patients with chronic granulomatous disease: case reports.

Bourdeaut F, Quartier P, Alkaer G, Fischer A, Casanova JL, Blanche S. Bourdeaut F, et al. Among authors: quartier p. Clin Infect Dis. 2002 Mar 15;34(6):853-4. doi: 10.1086/338875. Epub 2002 Jan 31. Clin Infect Dis. 2002. PMID: 11830798

8

Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes.

Feldmann J, Prieur AM, Quartier P, Berquin P, Certain S, Cortis E, Teillac-Hamel D, Fischer A, de Saint Basile G. Feldmann J, et al. Among authors: quartier p. Am J Hum Genet. 2002 Jul;71(1):198-203. doi: 10.1086/341357. Epub 2002 May 24. Am J Hum Genet. 2002. PMID: 12032915 Free PMC article.

9

Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis.

Feldmann J, Le Deist F, Ouachée-Chardin M, Certain S, Alexander S, Quartier P, Haddad E, Wulffraat N, Casanova JL, Blanche S, Fischer A, de Saint Basile G. Feldmann J, et al. Among authors: quartier p. Br J Haematol. 2002 Jun;117(4):965-72. doi: 10.1046/j.1365-2141.2002.03534.x. Br J Haematol. 2002. PMID: 12060139 Free article.

10

Immunodeficiency and genetic conditions that cause arthritis in childhood.

Quartier P, Prieur AM. Quartier P, et al. Curr Rheumatol Rep. 2002 Dec;4(6):483-93. doi: 10.1007/s11926-002-0054-5. Curr Rheumatol Rep. 2002. PMID: 12427362 Review.

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