Hemophagocytic Syndrome

Abstract Hemophagocytic syndrome is a life threatening condition characterized by uncontrolled hyperinflammation on the basis of various inherited or acquired immune deficiencies. We report a case of hemophagocytic syndrome in a 18 years old male with a brief review of literature.

Gespeichert in:

Autor*in:	Dhawale, Manjusha Shripad [verfasserIn] Joshi, Anil R. Bhatkule, Milind Anil Kumbhakarna, Neela Ratnakar Bindu, Rajan Shamrao

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2012

Schlagwörter:	Hemophagocytic syndrome Immunodeficiency

Anmerkung:	© Indian Society of Haematology & Transfusion Medicine 2012

Übergeordnetes Werk:	Enthalten in: Indian journal of hematology and blood transfusion - Neu Delhi : Springer India, 2007, 30(2012), Suppl 1 vom: 18. Dez., Seite 9-11
Übergeordnetes Werk:	volume:30 ; year:2012 ; number:Suppl 1 ; day:18 ; month:12 ; pages:9-11

Links:	Volltext

DOI / URN:	10.1007/s12288-012-0217-0

Katalog-ID:	SPR024797065

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allfields_unstemmed	10.1007/s12288-012-0217-0 doi (DE-627)SPR024797065 (SPR)s12288-012-0217-0-e DE-627 ger DE-627 rakwb eng Dhawale, Manjusha Shripad verfasserin aut Hemophagocytic Syndrome 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Indian Society of Haematology & Transfusion Medicine 2012 Abstract Hemophagocytic syndrome is a life threatening condition characterized by uncontrolled hyperinflammation on the basis of various inherited or acquired immune deficiencies. We report a case of hemophagocytic syndrome in a 18 years old male with a brief review of literature. Hemophagocytic syndrome (dpeaa)DE-He213 Immunodeficiency (dpeaa)DE-He213 Joshi, Anil R. aut Bhatkule, Milind Anil aut Kumbhakarna, Neela Ratnakar aut Bindu, Rajan Shamrao aut Enthalten in Indian journal of hematology and blood transfusion Neu Delhi : Springer India, 2007 30(2012), Suppl 1 vom: 18. Dez., Seite 9-11 (DE-627)564751227 (DE-600)2422370-0 0974-0449 nnns volume:30 year:2012 number:Suppl 1 day:18 month:12 pages:9-11 https://dx.doi.org/10.1007/s12288-012-0217-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 30 2012 Suppl 1 18 12 9-11
allfieldsGer	10.1007/s12288-012-0217-0 doi (DE-627)SPR024797065 (SPR)s12288-012-0217-0-e DE-627 ger DE-627 rakwb eng Dhawale, Manjusha Shripad verfasserin aut Hemophagocytic Syndrome 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Indian Society of Haematology & Transfusion Medicine 2012 Abstract Hemophagocytic syndrome is a life threatening condition characterized by uncontrolled hyperinflammation on the basis of various inherited or acquired immune deficiencies. We report a case of hemophagocytic syndrome in a 18 years old male with a brief review of literature. Hemophagocytic syndrome (dpeaa)DE-He213 Immunodeficiency (dpeaa)DE-He213 Joshi, Anil R. aut Bhatkule, Milind Anil aut Kumbhakarna, Neela Ratnakar aut Bindu, Rajan Shamrao aut Enthalten in Indian journal of hematology and blood transfusion Neu Delhi : Springer India, 2007 30(2012), Suppl 1 vom: 18. Dez., Seite 9-11 (DE-627)564751227 (DE-600)2422370-0 0974-0449 nnns volume:30 year:2012 number:Suppl 1 day:18 month:12 pages:9-11 https://dx.doi.org/10.1007/s12288-012-0217-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 30 2012 Suppl 1 18 12 9-11
allfieldsSound	10.1007/s12288-012-0217-0 doi (DE-627)SPR024797065 (SPR)s12288-012-0217-0-e DE-627 ger DE-627 rakwb eng Dhawale, Manjusha Shripad verfasserin aut Hemophagocytic Syndrome 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Indian Society of Haematology & Transfusion Medicine 2012 Abstract Hemophagocytic syndrome is a life threatening condition characterized by uncontrolled hyperinflammation on the basis of various inherited or acquired immune deficiencies. We report a case of hemophagocytic syndrome in a 18 years old male with a brief review of literature. Hemophagocytic syndrome (dpeaa)DE-He213 Immunodeficiency (dpeaa)DE-He213 Joshi, Anil R. aut Bhatkule, Milind Anil aut Kumbhakarna, Neela Ratnakar aut Bindu, Rajan Shamrao aut Enthalten in Indian journal of hematology and blood transfusion Neu Delhi : Springer India, 2007 30(2012), Suppl 1 vom: 18. Dez., Seite 9-11 (DE-627)564751227 (DE-600)2422370-0 0974-0449 nnns volume:30 year:2012 number:Suppl 1 day:18 month:12 pages:9-11 https://dx.doi.org/10.1007/s12288-012-0217-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 AR 30 2012 Suppl 1 18 12 9-11
language	English
source	Enthalten in Indian journal of hematology and blood transfusion 30(2012), Suppl 1 vom: 18. Dez., Seite 9-11 volume:30 year:2012 number:Suppl 1 day:18 month:12 pages:9-11
sourceStr	Enthalten in Indian journal of hematology and blood transfusion 30(2012), Suppl 1 vom: 18. Dez., Seite 9-11 volume:30 year:2012 number:Suppl 1 day:18 month:12 pages:9-11
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Hemophagocytic syndrome Immunodeficiency
isfreeaccess_bool	false
container_title	Indian journal of hematology and blood transfusion
authorswithroles_txt_mv	Dhawale, Manjusha Shripad @@aut@@ Joshi, Anil R. @@aut@@ Bhatkule, Milind Anil @@aut@@ Kumbhakarna, Neela Ratnakar @@aut@@ Bindu, Rajan Shamrao @@aut@@
publishDateDaySort_date	2012-12-18T00:00:00Z
hierarchy_top_id	564751227
id	SPR024797065
language_de	englisch
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author	Dhawale, Manjusha Shripad
spellingShingle	Dhawale, Manjusha Shripad misc Hemophagocytic syndrome misc Immunodeficiency Hemophagocytic Syndrome
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topic_title	Hemophagocytic Syndrome Hemophagocytic syndrome (dpeaa)DE-He213 Immunodeficiency (dpeaa)DE-He213
topic	misc Hemophagocytic syndrome misc Immunodeficiency
topic_unstemmed	misc Hemophagocytic syndrome misc Immunodeficiency
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title	Hemophagocytic Syndrome
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title_full	Hemophagocytic Syndrome
author_sort	Dhawale, Manjusha Shripad
journal	Indian journal of hematology and blood transfusion
journalStr	Indian journal of hematology and blood transfusion
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author_browse	Dhawale, Manjusha Shripad Joshi, Anil R. Bhatkule, Milind Anil Kumbhakarna, Neela Ratnakar Bindu, Rajan Shamrao
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author-letter	Dhawale, Manjusha Shripad
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title_sort	hemophagocytic syndrome
title_auth	Hemophagocytic Syndrome
abstract	Abstract Hemophagocytic syndrome is a life threatening condition characterized by uncontrolled hyperinflammation on the basis of various inherited or acquired immune deficiencies. We report a case of hemophagocytic syndrome in a 18 years old male with a brief review of literature. © Indian Society of Haematology & Transfusion Medicine 2012
abstractGer	Abstract Hemophagocytic syndrome is a life threatening condition characterized by uncontrolled hyperinflammation on the basis of various inherited or acquired immune deficiencies. We report a case of hemophagocytic syndrome in a 18 years old male with a brief review of literature. © Indian Society of Haematology & Transfusion Medicine 2012
abstract_unstemmed	Abstract Hemophagocytic syndrome is a life threatening condition characterized by uncontrolled hyperinflammation on the basis of various inherited or acquired immune deficiencies. We report a case of hemophagocytic syndrome in a 18 years old male with a brief review of literature. © Indian Society of Haematology & Transfusion Medicine 2012
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title_short	Hemophagocytic Syndrome
url	https://dx.doi.org/10.1007/s12288-012-0217-0
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author2	Joshi, Anil R. Bhatkule, Milind Anil Kumbhakarna, Neela Ratnakar Bindu, Rajan Shamrao
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up_date	2024-07-04T02:25:29.514Z
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