X-linked Lymphoproliferative Disease due to SAP/SH2D1A deficiency: A Multicentre Study on the manifestations, management and outcome of the disease

Booth, C; Gilmour, K; Veys, P; Gennery, A; Slatter, M; Chapel, H; Heath, P; Steward, C; Smith, O; O'Meara, A; Kerrigan, H; Mahlaoui, N; Cavazzana Calvo, M; Fischer, A; Moshous, D; Blanche, S; Pachlopnik Schmid, J; Latour, S; de Saint Basile, G; Albert, M; Notheis, G; Rieber, N; Strahm, B; Ritterbusch, H; Lankester, A; Hartwig, N; Meyts, I; Plebani, A; Soresina, A; Finocchi, A; Pignata, C; Cirillo, E; Bonanomi, S; Peters, C; Kalwak, K; Pasic, S; Sedlacek, P; Jazbec, J; Kanegane, H; Nichols, K; Hanson, I; Kapoor, N; Haddad, E; Cowan, M; Choo, S; Smart, J; Arkwright, P; Gaspar, H

doi:10.1182/blood-2010-06-284935

Booth, C., Gilmour, K., Veys, P., Gennery, A., Slatter, M., Chapel, H., et al. (2010). X-linked Lymphoproliferative Disease due to SAP/SH2D1A deficiency: A Multicentre Study on the manifestations, management and outcome of the disease. BLOOD, 117(1), 53-62 [10.1182/blood-2010-06-284935].

X-linked Lymphoproliferative Disease due to SAP/SH2D1A deficiency: A Multicentre Study on the manifestations, management and outcome of the disease

Booth, C;Gilmour, K;Veys, P;Gennery, A;Slatter, M;Chapel, H;Heath, P;Steward, C;Smith, O;O'Meara, A;Kerrigan, H;Mahlaoui, N;Cavazzana Calvo, M;Fischer, A;Moshous, D;Blanche, S;Pachlopnik Schmid, J;Latour, S;de Saint Basile, G;Albert, M;Notheis, G;Rieber, N;Strahm, B;Ritterbusch, H;Lankester, A;Hartwig, N;Meyts, I;Plebani, A;Soresina, A;FINOCCHI, ANDREA;Pignata, C;Cirillo, E;Bonanomi, S;Peters, C;Kalwak, K;Pasic, S;Sedlacek, P;Jazbec, J;Kanegane, H;Nichols, K;Hanson, I;Kapoor, N;Haddad, E;Cowan, M;Choo, S;Smart, J;Arkwright, P;Gaspar, H.

2010-06-01

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	Data di pubblicazione
	
			1-giu-2010
		
	Status di pubblicazione
	
			Pubblicato
		
	DOI dell'articolo
	
			https://dx.doi.org/10.1182/blood-2010-06-284935
		
	Rilevanza
	
			Rilevanza internazionale
		
	Tipo
	
			Articolo
		
	Referee
	
			Sì, ma tipo non specificato
		
	Settore disciplinare dell'articolo
	
			Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA
		
	Lingua del contenuto
	
			English
		
	Citazione
	
			Booth, C., Gilmour, K., Veys, P., Gennery, A., Slatter, M., Chapel, H., et al. (2010). X-linked Lymphoproliferative Disease due to SAP/SH2D1A deficiency: A Multicentre Study on the manifestations, management and outcome of the disease. BLOOD, 117(1), 53-62 [10.1182/blood-2010-06-284935].
		
	Tutti gli autori
	
			Booth, C; Gilmour, K; Veys, P; Gennery, A; Slatter, M; Chapel, H; Heath, P; Steward, C; Smith, O; O'Meara, A; Kerrigan, H; Mahlaoui, N; Cavazzana Calvo, M; Fischer, A; Moshous, D; Blanche, S; Pachlopnik Schmid, J; Latour, S; de Saint Basile, G; Albert, M; Notheis, G; Rieber, N; Strahm, B; Ritterbusch, H; Lankester, A; Hartwig, N; Meyts, I; Plebani, A; Soresina, A; Finocchi, A; Pignata, C; Cirillo, E; Bonanomi, S; Peters, C; Kalwak, K; Pasic, S; Sedlacek, P; Jazbec, J; Kanegane, H; Nichols, K; Hanson, I; Kapoor, N; Haddad, E; Cowan, M; Choo, S; Smart, J; Arkwright, P; Gaspar, H
		
	Tipologia
	
			Articolo su rivista
		
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