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Maximilian Heeg

Arzt

Name	Maximilian Heeg
Ort	Ulm (Geburtsort) Deutschland
Geschlecht	männlich
Akademischer Grad bzw. Titel	Dr. (an der Medizinischen Fakultät der Universität Freiburg (Breisgau)) (2015)
Beruf	Arzt (charakteristischer Beruf)
Datensatztyp	Person
GND-Nummer	107702374X
Datensatz-ID	107702374X
Beteiligt an alle anzeigen Retrospective identification of the first cord blood–transplanted severe aplastic anemia in a STAT1-associated chronic mucocutaneous candidiasis family : : case report, review of literature and pathophysiologic background JAKs and STATs from a clinical perspective: loss-of-function mutations, gain-of-function mutations, and their multidimensional consequences High antibody levels and reduced cellular response in children up to one year after SARS-CoV-2 infection Evaluation of Laboratory and Sonographic Parameters for Detection of Portal Hypertension in Patients with Common Variable Immunodeficiency High-dimensional profiling reveals Tc17 cell enrichment in active Crohn’s disease and identifies a potentially targetable signature Evaluation of laboratory and sonographic parameters for detection of portal hypertension in patients with common variable immunodeficiency High antibody levels and reduced cellular response in children up to one year after SARS-CoV-2 infection High-dimensional profiling reveals Tc17 cell enrichment in active Crohn’s disease and identifies a potentially targetable signature Therapeutic approaches to pediatric COVID-19: an online survey of pediatric rheumatologists A distinct CD38+CD45RA+ population of CD4+, CD8+, and double-negative T cells is controlled by FAS Germline STAT3 gain-of-function mutations in primary immunodeficiency: Impact on the cellular and clinical phenotype Therapeutic approaches to pediatric COVID-19: an online survey of pediatric rheumatologists Comprehensive infectious disease screening in a cohort of unaccompanied refugee minors in Germany from 2016 to 2017: a cross-sectional study COVID-19: Behandlungsstrategien der deutschsprachigen Kinderrheumatologen : : Ergebnisse einer Online-Umfrage Early-onset autoimmunity associated with SOCS1 haploinsufficiency Clinical and immunological phenotype of patients with primary immunodeficiency due to damaging mutations in NFKB2 The German National Registry of Primary Immunodeficiencies (2012-2017) The German National Registry of Primary Immunodeficiencies (2012-2017) The German national registry of primary immunodeficiencies (2012–2017) Disease evolution and response to rapamycin in activated phosphoinositide 3-kinase [delta] syndrome: the european society for immunodeficiencies-activated phosphoinositide 3-kinase [delta] syndrome registry Analyse der antiviralen Effektorfunktionen in einem neuen immunologischen Modell der HBV-Infektion

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Katalog der Deutschen Nationalbibliothek

Maximilian Heeg

Retrospective identification of the first cord blood–transplanted severe aplastic anemia in a STAT1-associated chronic mucocutaneous candidiasis family : : case report, review of literature and pathophysiologic background

JAKs and STATs from a clinical perspective: loss-of-function mutations, gain-of-function mutations, and their multidimensional consequences

High antibody levels and reduced cellular response in children up to one year after SARS-CoV-2 infection

Evaluation of Laboratory and Sonographic Parameters for Detection of Portal Hypertension in Patients with Common Variable Immunodeficiency

High-dimensional profiling reveals Tc17 cell enrichment in active Crohn’s disease and identifies a potentially targetable signature

Evaluation of laboratory and sonographic parameters for detection of portal hypertension in patients with common variable immunodeficiency

High antibody levels and reduced cellular response in children up to one year after SARS-CoV-2 infection

High-dimensional profiling reveals Tc17 cell enrichment in active Crohn’s disease and identifies a potentially targetable signature

Therapeutic approaches to pediatric COVID-19: an online survey of pediatric rheumatologists

A distinct CD38+CD45RA+ population of CD4+, CD8+, and double-negative T cells is controlled by FAS

Germline STAT3 gain-of-function mutations in primary immunodeficiency: Impact on the cellular and clinical phenotype

Therapeutic approaches to pediatric COVID-19: an online survey of pediatric rheumatologists

Comprehensive infectious disease screening in a cohort of unaccompanied refugee minors in Germany from 2016 to 2017: a cross-sectional study

COVID-19: Behandlungsstrategien der deutschsprachigen Kinderrheumatologen : : Ergebnisse einer Online-Umfrage

Early-onset autoimmunity associated with SOCS1 haploinsufficiency

Clinical and immunological phenotype of patients with primary immunodeficiency due to damaging mutations in NFKB2

The German National Registry of Primary Immunodeficiencies (2012-2017)

The German National Registry of Primary Immunodeficiencies (2012-2017)

The German national registry of primary immunodeficiencies (2012–2017)

Disease evolution and response to rapamycin in activated phosphoinositide 3-kinase [delta] syndrome: the european society for immunodeficiencies-activated phosphoinositide 3-kinase [delta] syndrome registry

Analyse der antiviralen Effektorfunktionen in einem neuen immunologischen Modell der HBV-Infektion