B. Belohradsky

发表

Chronic recurrent multifocal osteomyelitis (CRMO).

H. Dietz, T. Schuster, J. Bielek, 1996, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Inflammatory pseudotumor (IPT)—surgical cure of an inflammatory syndrome

D. Horst, T. Pfluger, U. Wintergerst, 2016, European Journal of Pediatrics.

Chronic granulomatous disease in adults

M. Gahr, J. Liese, V. Jendrossek, 1996, The Lancet.

Airway inflammation in children with tracheostomy

T. Nicolai, K. Reid, M. Griese, 2004, Pediatric pulmonology.

Posaconazole for treatment of refractory invasive fungal disease

J. Rosenecker, D. Reinhardt, U. Wintergerst, 2006, Mycoses.

[Pasini and Pierini idiopathic and progressive atrophoderma in childhood].

L. Barran, B. Belohradsky, S. Kellnar, 1986, Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde.

Bacterial endophthalmitis in neonates

B. Belohradsky, R. Lohrer, 1987, European Journal of Pediatrics.

[Recurring disseminated Mycobacterium avium infections in an HIV-negative patient].

F. Gamarra, M. Krötz, J. Bogner, 2005, Deutsche medizinische Wochenschrift.

Therapy of focal viral encephalitis in children with aciclovir and recombinant beta-interferon - results of a placebo-controlled multicenter study.

T. Pfluger, U. Wintergerst, B. Belohradsky, 2005, European journal of medical research.

Pyonephrosis in childhood — Is ultrasound sufficient for diagnosis?

H. Fendel, K. Devens, B. Belohradsky, 2006, Pediatric Radiology.

Natural killer cell function and interferon production in familial hemophagocytic lymphohistiocytosis.

H. Holtmann, B. Belohradsky, G. Janka, 1989, Pediatric hematology and oncology.

Celiac disease and pulmonary hemosiderosis in a patient with chronic granulomatous disease

T. Nicolai, M. Griese, D. Roos, 2004, Pediatric pulmonology.

Impaired cellular immune response to diphtheria and tetanus vaccines in children after thoracic transplantation

S. Urschel, N. Rieber, K. Januszewska, 2011, Pediatric transplantation.

Treatment of relapsing Mycobacterium avium infection with interferon-gamma and interleukin-2 in an HIV-negative patient with low CD4 syndrome.

J. Bogner, B. Belohradsky, A. Nigg, 2010, International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases.

[Rational use of oral antibiotics in children and young people. Findings of an expert commission of the Paul Ehrlich Society for Chemotherapy ].

R. Roos, W. Handrick, U. Heininger, 2002, Medizinische Monatsschrift fur Pharmazeuten.

A new low‐penetrance TNFRSF1A mutation causing atypical periodic fever

B. Belohradsky, P. Lohse, B. Belohradsky, 2006, Pediatrics international : official journal of the Japan Pediatric Society.

INFANTILE CHRONIC RELAPSING INFLAMMATION OF THE BRAIN, SKIN, AND JOINTS

F. Lampert, P. Lampert, B. Belohradsky, 1975, The Lancet.

Genetic linkage of hyper-IgE syndrome to chromosome 4.

A. Schäffer, S. Holland, H. Ochs, 1999, American journal of human genetics.

BTKbase, mutation database for X-linked agammaglobulinemia (XLA)

Mauno Vihinen, Christine Kinnon, Igor Vorechovsky, 1996, Nucleic Acids Res..

Chronic Granulomatous Disease: The European Experience

Dirk Roos, Theoni Petropoulou, A. Fischer, 2009, PloS one.

Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome)

G. Gimelli, İ. Reisli, A. Gennery, 2007, Journal of Medical Genetics.

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes.

A. Schäffer, E. Gertz, A. Plebani, 2008, Blood.

Lupus erythematosus tumidus and chronic discoid lupus erythematosus in carriers of X-linked chronic granulomatous disease.

R. Rupec, J. Liese, B. Belohradsky, 2000, European journal of dermatology : EJD.

X-linked inhibitor of apoptosis (XIAP) deficiency: the spectrum of presenting manifestations beyond hemophagocytic lymphohistiocytosis.

K. Schwarz, S. Ehl, H. von Bernuth, 2013, Clinical immunology.

Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP).

W. Friedrich, A. Meindl, H. Hellebrand, 1999, Human molecular genetics.

Dyskeratosis congenita

B. Belohradsky, B. Sölder, M. Weiss, 1996, Klinische Padiatrie.

Comèl-Netherton syndrome defined as primary immunodeficiency.

J. Orange, H. Ochs, T. Torgerson, 2009, The Journal of allergy and clinical immunology.