B. H. Belohradsky - Concepedia

Author

B. H. Belohradsky

Also Known As

B Belohradsky, B H Belohradsky, B. Belohradsky, B. H. BELOHRADSKY, B. H. Belohradsky, B.H Belohradsky, B.H. Belohradsky, BH Belohradsky

157

Publications

Citations

H-Index

123

Concepts

All Affiliations

Ludwig-Maximilians-Universität München Universitätskinderklinik München Klinik University College London LMU Klinikum

About

B. H. Belohradsky is an author at Ludwig-Maximilians-Universität München specializing in medicine, pediatrics, and immunology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	33	2.8K
2	Health Sciences	2	2	113
3	Allergy	2	2	207
4	Natural Sciences	1	1	86
5	Public Health	1	1	81

B. H. Belohradsky

Publications

4.5K

Citations

H-Index

Page 1

	Year	Citations
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. A K Ryan, Judith A. Goodship, David I. Wilson, Journal of Medical Genetics CytogeneticsGeneticsGenetic EpidemiologyEuropean Collaborative StudyPathology	1997	1.2K
Classification of Non-Bacterial Osteitis: Retrospective study of clinical, immunological and genetic aspects in 89 patients Annette Jansson, Ellen D. Renner, Juliane Ramser, Lara D. Veeken	2006	466
Pyrrolidine dithiocarbamate inhibits NF-<i>kappa</i> B mobilization and TNF production in human monocytes. H.W.L. Ziegler-Heitbrock, Thomas Sternsdorf, Johannes G. Liese, The Journal of Immunology	1993	305
Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome) Melanie M. Hagleitner, Arjan C. Lankester, P Maraschio, Journal of Medical Genetics	2007	215
X-linked inhibitor of apoptosis (XIAP) deficiency: The spectrum of presenting manifestations beyond hemophagocytic lymphohistiocytosis Carsten Speckmann, Kai Lehmberg, Michael H. Albert, Clinical Immunology Autoimmune DiseaseApoptosisHematologyImmunologyCell Death	2013	170
A primary T-cell immunodeficiency associated with defective transmembrane calcium influx Françoise Le Deist, Claire Hivroz, Michel Partiseti, Blood	1995	169
Chronic granulomatous disease in adults Johannes G. Liese, Annette Jansson, Th Petropoulou, The Lancet Pulmonary PathologyChronic Granulomatous DiseaseGranulocytePathologyDermatopathology	1996	144
A human immunodeficiency syndrome caused by mutations in CARMIL2 Tilmann Schober, Thomas Magg, Melanie Laschinger, Nature Communications	2017	123
Efficacy and safety of Hizentra® in patients with primary immunodeficiency after a dose-equivalent switch from intravenous or subcutaneous replacement therapy Stephen Jolles, Ewa Bernatowska, Javier de Gracia, Clinical Immunology Subcutaneous InfusionsImmunodeficienciesPharmacotherapyDermatologyImmunotherapy	2011	117
Epstein--Barr Virus-Negative Boys With Non-Hodgkin Lymphoma Are Mutated in the Sh2D1A Gene, as Are Patients With X-Linked Lymphoproliferative Disease (XLP) Oliver Brandau, Volker Schuster, Michael Weiss, Human Molecular Genetics ImmunodeficienciesGeneticsImmunologyPathologySh2d1a Gene	1999	107

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