Works matching AU Henter, Jan-Inge

Results: 108

Diagnostic challenges for a novel SH2D1A mutation associated with X-linked lymphoproliferative disease.

Published in:

2020

By:

Torralba‐Raga, Lamberto;
Tesi, Bianca;
Chiang, Samuel C. C.;
Schlums, Heinrich;
Nordenskjöld, Magnus;
Horne, AnnaCarin;
Henter, Jan‐Inge;
Meeths, Marie;
Abdelhaleem, Mohamed;
Weitzman, Sheila;
Bryceson, Yenan;
Torralba-Raga, Lamberto;
Henter, Jan-Inge

Publication type:

journal article

Haploinsufficiency of UNC13D increases the risk of lymphoma.

Published in:

2019

By:

Löfstedt, Alexandra;
Ahlm, Clas;
Tesi, Bianca;
Bergdahl, Ingvar A.;
Nordenskjöld, Magnus;
Bryceson, Yenan T.;
Henter, Jan‐Inge;
Meeths, Marie;
Henter, Jan-Inge

Publication type:

journal article

Therapeutic administration of etoposide coincides with reduced systemic HMGB1 levels in macrophage activation syndrome.

Published in:

Molecular Medicine, 2021, v. 27, n. 1, p. 1, doi. 10.1186/s10020-021-00308-0

By:

Palmblad, Karin;
Schierbeck, Hanna;
Sundberg, Erik;
Horne, Anna-Carin;
Erlandsson Harris, Helena;
Henter, Jan-Inge;
Andersson, Ulf

Publication type:

Article

Retraction Note to: High systemic levels of the cytokine-inducing HMGB1 isoform secreted in severe macrophage activation syndrome.

Published in:

Molecular Medicine, 2020, v. 26, n. 1, p. 1, doi. 10.1186/s10020-020-00263-2

By:

Palmblad, Karin;
Schierbeck, Hanna;
Sundberg, Erik;
Horne, Anna-Carin;
Harris, Helena Erlandsson;
Henter, Jan-Inge;
Antoine, Daniel J.;
Andersson, Ulf

Publication type:

Article

OP009. Stromal Cell - Innate Immune Cell Interactions in Pediatric Inflammatory Bowel Disease Patients.

Published in:

Journal of Pediatric Gastroenterology & Nutrition, 2017, v. 65, p. S5

By:

Kvedaraite, Egle;
Lourda, Magda;
Van Acker, Aline;
Jess, David Unnersjö;
Gavhed, Désirée;
Mjösberg, Jenny;
Ideström, Maja;
Henter, Jan-Inge;
Svensson, Mattias

Publication type:

Article

Evaluation of Parvovirus B19 Infection in Children with Malignant or Hematological Disorders.

Published in:

2010

By:

Gustafsson, Igge;
Kaldensjö, Tove;
Lindblom, Anna;
Norbeck, Oscar;
Henter, Jan-Inge;
Tolfvenstam, Thomas;
Broliden, Kristina

Publication type:

Letter

Parvovirus B19 Infection in Children with Acute Lymphoblastic Leukemia Is Associated with Cytopenia Resulting in Prolonged Interruptions of Chemotherapy.

Published in:

Clinical Infectious Diseases, 2008, v. 46, n. 4, p. 528, doi. 10.1086/526522

By:

Lindblom, Anna;
Heyman, Mats;
Gustafsson, Igge;
Norbeck, Oscar;
Kaldensjö,, Tove;
Vernby, Åsa;
Henter, Jan-Inge;
Lolfvenstam, Thomas;
Broliden, Kristina

Publication type:

Article

SAMHD1 protects cancer cells from various nucleoside-based antimetabolites.

Published in:

Cell Cycle, 2017, v. 16, n. 11, p. 1029, doi. 10.1080/15384101.2017.1314407

By:

Herold, Nikolas;
Rudd, Sean G.;
Sanjiv, Kumar;
Kutzner, Juliane;
Bladh, Julia;
Paulin, Cynthia B. J.;
Helleday, Thomas;
Henter, Jan-Inge;
Schaller, Torsten

Publication type:

Article

An N-terminal missense mutation in STX11 causative of FHL4 abrogates syntaxin-11 binding to Munc18-2.

Published in:

Frontiers in Immunology, 2014, v. 4, p. 1, doi. 10.3389/fimmu.2013.00515

By:

Müller, Martha-Lena;
Chiang, Samuel C. C.;
Meeths, Marie;
Tesi, Bianca;
Entesarian, Miriam;
Nilsson, Daniel;
Wood, Stephanie M.;
Nordenskjöld, Magnus;
Henter, Jan-Inge;
Naqvi, Ahmed;
Bryceson, Yenan T.

Publication type:

Article

Familial Hemophagocytic Lymphohistiocytosis: Too Little Cell Death Can Seriously Damage Your Health.

Published in:

Leukemia & Lymphoma, 2001, v. 42, n. 1/2, p. 13, doi. 10.3109/10428190109097672

By:

Fadeel, Bengt;
Orrenius, Sten;
Henter, Jan-Inge

Publication type:

Article

Dengue Infection Complicated by Hemophagocytic Lymphohistiocytosis: Experiences From 180 Patients With Severe Dengue.

Published in:

Clinical Infectious Diseases, 2020, v. 70, n. 11, p. 2247, doi. 10.1093/cid/ciz499

By:

Kan, Foong Kee;
Tan, Cheng Cheng;
Greenwood, Tatiana Von Bahr;
Khalid, Khairil E;
Supramaniam, Premaa;
Myrberg, Ida Hed;
Tan, Lian Huat;
Henter, Jan-Inge

Publication type:

Article

The ECHO recommendations for dealing with vinblastine shortage affecting standard treatment of systemic Langerhans cell histiocytosis.

Published in:

Pediatric Blood & Cancer, 2024, v. 71, n. 3, p. 1, doi. 10.1002/pbc.30850

By:

Papadakis, Vassilios;
Astigarraga, Itziar;
van den Bos, Cor;
Donadieu, Jean;
Henter, Jan‐Inge;
Jacobs, Sandra;
Lehrnbecher, Thomas;
Munthe‐Kaas, Monica Cheng;
Naeije, Leonie;
Nanduri, Vasanta;
Nguyen, Trung;
Nysom, Karsten;
Pears, Jane;
Raciborska, Anna;
Sieni, Elena;
Svojgr, Karel;
Tzotzola, Vasiliki;
Minkov, Milen

Publication type:

Article

Is neutralization of IFN‐γ sufficient to control inflammation in HLH?

Published in:

Pediatric Blood & Cancer, 2021, v. 68, n. 3, p. 1, doi. 10.1002/pbc.28886

By:

Ehl, Stephan;
von Bahr Greenwood, Tatiana;
Bergsten, Elisabet;
Fischer, Alain;
Henter, Jan‐Inge;
Hines, Melissa;
Lehmberg, Kai;
Janka, Gritta;
Moshous, Despina;
Nichols, Kim E.

Publication type:

Article

Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense Mutations.

Published in:

2015

By:

Tesi, Bianca;
Chiang, Samuel C. C.;
El‐Ghoneimy, Dalia;
Hussein, Ayad Ahmed;
Langenskiöld, Cecilia;
Wali, Rabia;
Fadoo, Zehra;
Silva, João Pinho;
Lecumberri, Ramón;
Unal, Sule;
Nordenskjöld, Magnus;
Bryceson, Yenan T.;
Henter, Jan‐Inge;
Meeths, Marie

Publication type:

journal article

Incidence and clinical presentation of primary hemophagocytic lymphohistiocytosis in Sweden.

Published in:

2015

By:

Meeths, Marie;
Horne, AnnaCarin;
Sabel, Magnus;
Bryceson, Yenan T.;
Henter, Jan‐Inge

Publication type:

journal article

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).

Published in:

Nature Genetics, 2007, v. 39, n. 1, p. 86, doi. 10.1038/ng1940

By:

Klein, Christoph;
Grudzien, Magda;
Appaswamy, Giridharan;
Germeshausen, Manuela;
Sandrock, Inga;
Schäffer, Alejandro A.;
Rathinam, Chozhavendan;
Boztug, Kaan;
Schwinzer, Beate;
Rezaei, Nima;
Bohn, Georg;
Melin, Malin;
Carlsson, Göran;
Fadeel, Bengt;
Dahl, Niklas;
Palmblad, Jan;
Henter, Jan-Inge;
Zeidler, Cornelia;
Grimbacher, Bodo;
Welte, Karl

Publication type:

Article

Killer cell immunoglobulin-like receptor gene polymorphisms predispose susceptibility to Epstein-Barr virus associated hemophagocytic lymphohistiocytosis in Chinese children.

Published in:

Microbiology & Immunology, 2012, v. 56, n. 6, p. 378, doi. 10.1111/j.1348-0421.2012.00443.x

By:

Qiang, Qin;
Zhengde, Xie;
Chunyan, Liu;
Zhizhuo, Huang;
Junmei, Xu;
Junhong, Ai;
Zheng, Chengyun;
Henter, Jan-Inge;
Kunling, Shen

Publication type:

Article

Molecular Genetics Diversity of Primary Hemophagocytic Lymphohistiocytosis among Polish Pediatric Patients.

Published in:

Archivum Immunologiae & Therapiae Experimentalis, 2021, v. 69, n. 1, p. 1, doi. 10.1007/s00005-021-00635-4

By:

Bąbol-Pokora, Katarzyna;
Wołowiec, Magdalena;
Popko, Katarzyna;
Jaworowska, Aleksandra;
Bryceson, Yenan T.;
Tesi, Bianca;
Henter, Jan-Inge;
Młynarski, Wojciech;
Badowska, Wanda;
Balwierz, Walentyna;
Drabko, Katarzyna;
Kałwak, Krzysztof;
Maciejka-Kembłowska, Lucyna;
Pieczonka, Anna;
Sobol-Milejska, Grażyna;
Kołtan, Sylwia;
Malinowska, Iwona

Publication type:

Article

Syntaxin 11 marks a distinct intracellular compartment recruited to the immunological synapse of NK cells to colocalize with cytotoxic granules.

Published in:

Journal of Cellular & Molecular Medicine, 2012, v. 16, n. 1, p. 129, doi. 10.1111/j.1582-4934.2011.01280.x

By:

Dabrazhynetskaya, Alena;
Ma, Jinxia;
Guerreiro-Cacais, Andre Ortlieb;
Arany, Zita;
Rudd, Eva;
Henter, Jan-Inge;
Karre, Klas;
Levitskaya, Jelena;
Levitsky, Victor

Publication type:

Article

Novel deep intronic and missense UNC13 D mutations in familial haemophagocytic lymphohistiocytosis type 3.

Published in:

British Journal of Haematology, 2013, v. 162, n. 3, p. 415, doi. 10.1111/bjh.12371

By:

Entesarian, Miriam;
Chiang, Samuel C. C.;
Schlums, Heinrich;
Meeths, Marie;
Chan, Mei‐Yoke;
Mya, Soe‐Nwe;
Soh, Shui‐Yen;
Nordenskjöld, Magnus;
Henter, Jan‐Inge;
Bryceson, Yenan T.

Publication type:

Article

Incidence of severe congenital neutropenia in Sweden and risk of evolution to myelodysplastic syndrome/leukaemia.

Published in:

British Journal of Haematology, 2012, v. 158, n. 3, p. 363, doi. 10.1111/j.1365-2141.2012.09171.x

By:

Carlsson, Göran;
Fasth, Anders;
Berglöf, Elisabet;
Lagerstedt-Robinson, Kristina;
Nordenskjöld, Magnus;
Palmblad, Jan;
Henter, Jan-Inge;
Fadeel,, Bengt

Publication type:

Article

Multiple inherited sequence variations in two disease-causing genes in familial haemophagocytic lymphohistiocytosis.

Published in:

2009

By:

Rudd, Eva;
Meeths, Marie;
Uysal, Zümrüt;
Nordenskjöld, Magnus;
Henter, Jan-Inge;
Fadeel, Bengt

Publication type:

Letter

Characterization of PRF1, STX11 and UNC13D genotype-phenotype correlations in familial hemophagocytic lymphohistiocytosis.

Published in:

British Journal of Haematology, 2008, v. 143, n. 1, p. 75, doi. 10.1111/j.1365-2141.2008.07315.x

By:

Horne, AnnaCarin;
Ramme, Kim Göransdotter;
Rudd, Eva;
Chengyun Zheng;
Wali, Yasser;
al-Lamki, Zakia;
Gürgey, Aytemiz;
Yalman, Nevin;
Nordenskjöld, Magnus;
Henter, Jan-Inge

Publication type:

Article

Syntaxin-11 is expressed in primary human monocytes/macrophages and acts as a negative regulator of macrophage engulfment of apoptotic cells and IgG-opsonized target cells.

Published in:

British Journal of Haematology, 2008, v. 142, n. 3, p. 469, doi. 10.1111/j.1365-2141.2008.07191.x

By:

Zhang, Shouting;
Ma, Daoxin;
Wang, Xiangling;
Celkan, Tiraje;
Nordenskjöld, Magnus;
Henter, Jan-Inge;
Fadeel, Bengt;
Zheng, Chengyun

Publication type:

Article

Frequency and spectrum of central nervous system involvement in 193 children with haemophagocytic lymphohistiocytosis.

Published in:

British Journal of Haematology, 2008, v. 140, n. 3, p. 327, doi. 10.1111/j.1365-2141.2007.06922.x

By:

Horne, AnnaCarin;
Trottestam, Helena;
Aricò, Maurizio;
Egeler, R. Maarten;
Filipovich, Alexandra H.;
Gadner, Helmut;
Imashuku, Shinsaku;
Ladisch, Stephan;
Webb, David;
Janka, Gritta;
Henter, Jan-Inge

Publication type:

Article

Low plasma levels of the protein pro-LL-37 as an early indication of severe disease in patients with chronic neutropenia.

Published in:

British Journal of Haematology, 2007, v. 137, n. 2, p. 166, doi. 10.1111/j.1365-2141.2007.06530.x

By:

Karlsson, Jenny;
Carlsson, Göran;
Ramme, Kim Göransdotter;
Hägglund, Hans;
Fadeel, Bengt;
Nordenskjöld, Magnus;
Henter, Jan-Inge;
Palmblad, Jan;
Pütsep, Katrin;
Andersson, Mats

Publication type:

Article

Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis.

Published in:

British Journal of Haematology, 2005, v. 129, n. 5, p. 622, doi. 10.1111/j.1365-2141.2005.05501.x

By:

Horne, AnnaCarin;
Janka, Gritta;
Maarten Egeler, R.;
Gadner, Helmut;
Imashuku, Shinsaku;
Ladisch, Stephan;
Locatelli, Franco;
Montgomery, Scott M.;
Webb, David;
Winiarski, Jacek;
Filipovich, Alexandra H.;
Henter, Jan-Inge

Publication type:

Article

Subtyping of natural killer cell cytotoxicity deficiencies in haemophagocytic lymphohistocytosis provides therapeutic guidance.

Published in:

British Journal of Haematology, 2005, v. 129, n. 5, p. 658, doi. 10.1111/j.1365-2141.2005.05502.x

By:

Horne, AnnaCarin;
Zheng, Chengyun;
Lorenz, Ingrid;
Löfstedt, Martina;
Montgomery, Scott M.;
Janka, Gritta;
Henter, Jan-Inge;
Marion Schneider, E.

Publication type:

Article

Efficacy and safety of two different rG-CSF preparations in the treatment of patients with severe congenital neutropenia.

Published in:

British Journal of Haematology, 2004, v. 126, n. 1, p. 127, doi. 10.1111/j.1365-2141.2004.05008.x

By:

Carlsson, Göram;
Åhlin, Anders;
Dahllöf, Göran;
Elinder, Göran;
Henter, Jan-Inge;
Palmblad, Jan

Publication type:

Article

Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RPS19) gene.

Published in:

British Journal of Haematology, 2002, v. 119, n. 1, p. 261, doi. 10.1046/j.1365-2141.2002.03776.x

By:

Gustavsson, Peter;
Klar, Joakim;
Matsson, Hans;
Forestier, Erik;
Henter, Jan-Inge;
Rao, Sreedhar;
Seip, Martin;
Skeppner, Gunnar;
Dahl, Niklas

Publication type:

Article

2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation Collaborative Initiative

Published in:

Arthritis & Rheumatology, 2016, v. 68, n. 3, p. 566, doi. 10.1002/art.39332

By:

Ravelli, Angelo;
Minoia, Francesca;
Davì, Sergio;
Horne, AnnaCarin;
Bovis, Francesca;
Pistorio, Angela;
Aricò, Maurizio;
Avcin, Tadej;
Behrens, Edward M.;
De Benedetti, Fabrizio;
Filipovic, Lisa;
Grom, Alexei A.;
Henter, Jan‐Inge;
Ilowite, Norman T.;
Jordan, Michael B.;
Khubchandani, Raju;
Kitoh, Toshiyuki;
Lehmberg, Kai;
Lovell, Daniel J.;
Miettunen, Paivi

Publication type:

Article

Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 6, p. 827, doi. 10.1093/hmg/ddi076

By:

zur Stadt, Udo;
Schmidt, Susanne;
Kasper, Brigitte;
Beutel, Karin;
Diler, A. Sarper;
Henter, Jan-Inge;
Kabisch, Hartmut;
Schneppenheim, Reinhard;
Nürnberg, Peter;
Janka, Gritta;
Hennies, Hans Christian

Publication type:

Article

Induction of apoptosis and caspase activation in cells obtained from familial haemophagocytic lymphohistiocytosis patients.

Published in:

British Journal of Haematology, 1999, v. 106, n. 2, p. 406, doi. 10.1046/j.1365-2141.1999.01538.x

By:

Fadeel, Bengt;
Orrenius, Sten;
Henter, Jan-Inge

Publication type:

Article

HAEMOPHAGOCYTICLYMPHOHISTIOCYTOSIS: AN INHERITED PRIMARY FORM AND A REACTIVE SECONDARY FORM.

Published in:

British Journal of Haematology, 1995, v. 91, n. 3, p. 774, doi. 10.1111/j.1365-2141.1995.tb05386.x

By:

Henter, Jan-Inge;
Elinder, Goran

Publication type:

Article

Targeting BCL2 Family in Human Myeloid Dendritic Cells: A Challenge to Cure Diseases with Chronic Inflammations Associated with Bone Loss.

Published in:

2013

By:

Olsson Åkefeldt, Selma;
Ismail, Mohamad Bachar;
Valentin, Hélène;
Aricò, Maurizio;
Henter, Jan-Inge;
Delprat, Christine

Publication type:

Journal Article

Simultaneous manifestation of fulminant infectious mononucleosis with haemophagocytic syndrome and B-cell lymphoma in X-linked lymphoproliferative disease.

Published in:

2007

By:

Hügle, B.;
Astigarraga, I.;
Henter, J.-I.;
Porwit-MacDonald, A.;
Meindl, A.;
Schuster, Volker;
Hügle, Boris;
Astigarraga, Itziar;
Henter, Jan-Inge;
Porwit-MacDonald, Anna;
Meindl, Alfons

Publication type:

journal article

Betulinic acid, a natural cytotoxic agent, fails to trigger apoptosis in human Burkitt's lymphoma-derived B-cell lines.

Published in:

International Journal of Cancer, 2006, v. 118, n. 1, p. 246, doi. 10.1002/ijc.21311

By:

Karpova, Maria B.;
Sanmun, Duangmanee;
Henter, Jan-Inge;
Smirnov, Aleksandr F.;
Fadeel, Bengt

Publication type:

Article

Severe bacteria-associated hemophagocytic lymphohistiocytosis in an extremely premature infant.

Published in:

Acta Paediatrica, 2007, v. 96, n. 11, p. 1703, doi. 10.1111/j.1651-2227.2007.00505.x

By:

Edner, Josefine;
Rudd, Eva;
Chengyun Zheng;
Dahlander, Andreas;
Eksborg, Staffan;
Schneider, E Marion;
Edner, Ann;
Henter, Jan-Inge

Publication type:

Article

Kostmann syndrome or infantile genetic agranulocytosis, part two: understanding the underlying genetic defects in severe congenital neutropenia.

Published in:

Acta Paediatrica, 2007, v. 96, n. 6, p. 813, doi. 10.1111/j.1651-2227.2007.00274.x

By:

Carlsson, Göran;
Melin, Malin;
Dahl, Niklas;
Ramme, Kim Göransdotter;
Nordenskjöld, Magnus;
Palmblad, Jan;
Henter, Jan-Inge;
Fadeel, Bengt

Publication type:

Article

Kostmann syndrome or infantile genetic agranulocytosis, part one: celebrating 50 years of clinical and basic research on severe congenital neutropenia.

Published in:

2006

By:

Carlsson, Göran;
Andersson, Mats;
Pütsep, Katrin;
Garwicz, Daniel;
Nordenskjöld, Magnus;
Henter, Jan-Inge;
Palmblad, Jan;
Fadeel, Bengt;
Carlsson, Göran;
Pütsep, Katrin;
Nordenskjöld, Magnus

Publication type:

journal article

Long-term follow-up of Langerhans cell histiocytosis: 39 years' experience at a single centre.

Published in:

2005

By:

Bernstrand, Cecilia;
Sandstedt, Bengt;
Åhström, Lars;
Henter, Jan-Inge;
Ahström, Lars

Publication type:

journal article

Childhood idiopathic thrombocytopenic purpura in the Nordic countries: epidemiology and predictors of chronic disease.

Published in:

2005

By:

Zeller, Bernward;
Rajantie, Jukka;
Hedlund-Treutiger, Iris;
Tedgård, Ulf;
Wesenberg, Finn;
Jonsson, Olafur G.;
Henter, Jan Inge;
RosthØj, Steen;
Tedgård, Ulf;
NOPHO ITP

Publication type:

journal article

Kala-azar in a one-year-old Swedish child. Diagnostic difficulties because of active hemophagocytosis.

Published in:

Acta Paediatrica, 1993, v. 82, n. 10, p. 794, doi. 10.1111/j.1651-2227.1993.tb12562.x

By:

Granert, Carl;
Elinder, Göran;
Öst, Åke;
Henter, Jan-Inge

Publication type:

Article

Lipoprotein alterations in children with bacterial meningitis.

Published in:

Acta Paediatrica, 1993, v. 82, n. 9, p. 694, doi. 10.1111/j.1651-2227.1993.tb12793.x

By:

Henter, Jan-Inge;
Carlson, Lars A;
Hansson, Mona;
Nilsson-Ehle, Peter;
Örtqvist, Eva

Publication type:

Article

Lipoprotein alterations in children with bacterial meningitis.

Published in:

1993

By:

Henter, Jan-Inge;
Carlson, Lars A.;
Hansson, Mona;
Nilsson-Ehle, Peter;
Örtqvist, Eva;
Henter, J I;
Carlson, L A;
Hansson, M;
Nilsson-Ehle, P;
Ortqvist, E

Publication type:

journal article

Familial hemophagocytic lymphohistiocytosis and viral infections.

Published in:

1993

By:

Henter, Jan-Inge;
Ehrnst, Anneka;
Andersson, Jan;
Elinder, Göran;
Henter, J I;
Ehrnst, A;
Andersson, J;
Elinder, G

Publication type:

journal article

Lipoprotein Alterations and Plasma Lipoprotein Lipase Reduction in Familial Hemophagocytic Lymphohistiocytosis.

Published in:

Acta Paediatrica, 1991, v. 80, n. 6/7, p. 675, doi. 10.1111/j.1651-2227.1991.tb11928.x

By:

HENTER, JAN-INGE;
CARLSON, LARS A.;
SÖDER, OLLE;
NILSSON-EHLE, PETER;
ELINDER, GÖRAN

Publication type:

Article

Incidence in Sweden and Clinical Features of Familial Hemophagocytic Lymphohistiocytosis.

Published in:

Acta Paediatrica, 1991, v. 80, n. 4, p. 428, doi. 10.1111/j.1651-2227.1991.tb11878.x

By:

HENTER, JAN-INGE;
ELINDER, GÖRAN;
SÖDER, OLLE;
ÖST, ÅKE

Publication type:

Article

Familial Hemophagocytic Lymphohistiocytosis: Clinical Review Based on the Findings in Seven Children.

Published in:

Acta Paediatrica, 1991, v. 80, n. 3, p. 269, doi. 10.1111/j.1651-2227.1991.tb11849.x

By:

HENTER, JAN-INGE;
ELINDER, GÖRAN

Publication type:

Article

Prenatal diagnosis of perforin gene mutations in familial hemophagocytic lymphohistiocytosis (FHLH).

Published in:

2002

By:

zur Stadt, Udo;
Pruggmayer, Michael;
Jung, Helena;
Henter, Jan-Inge;
Schneider, Marion;
Kabisch, Hartmut;
Janka, Gritta

Publication type:

Case Study