Pages that link to "Q95335474"
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The following pages link to Manfred Gahr (Q95335474):
Displaying 50 items.
- Cultural bias in the AAP's 2012 Technical Report and Policy Statement on male circumcision (Q28287501) (← links)
- Naturally occurring genetic variants of human caspase-1 differ considerably in structure and the ability to activate interleukin-1β. (Q30419673) (← links)
- Early diagnosis of neonatal infection (Q33460552) (← links)
- Listeria monocytogenes and recurrent mycobacterial infections in a child with complete interferon-gamma-receptor (IFNgammaR1) deficiency: mutational analysis and evaluation of therapeutic options (Q33729982) (← links)
- Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p. (Q35070451) (← links)
- Defective removal of ribonucleotides from DNA promotes systemic autoimmunity. (Q35242453) (← links)
- Early onset systemic lupus erythematosus: differential diagnoses, clinical presentation, and treatment options. (Q37795641) (← links)
- Alu-repeat-induced deletions within the NCF2 gene causing p67-phox-deficient chronic granulomatous disease (CGD). (Q39768422) (← links)
- Fetal Properties in Red Blood Cells of Newborn Infants (Q39903006) (← links)
- A mutation in TREX1 that impairs susceptibility to granzyme A-mediated cell death underlies familial chilblain lupus (Q40144366) (← links)
- P-glycoprotein expression increases ATP release in respiratory cystic fibrosis cells (Q40407780) (← links)
- Periodic fever, mild arthralgias, and reversible moderate and severe organ inflammation associated with the V198M mutation in the CIAS1 gene in three German patients--expanding phenotype of CIAS1 related autoinflammatory syndrome (Q40530190) (← links)
- Two German CINCA (NOMID) patients with different clinical severity and response to anti-inflammatory treatment (Q40551844) (← links)
- Periodic fever (TRAPS) caused by mutations in the TNFalpha receptor 1 (TNFRSF1A) gene of three German patients (Q40592903) (← links)
- Clinical experience of a tricomponent acellular pertussis vaccine combined with diphtheria and tetanus toxoids for primary vaccination in 22,505 infants (Q40662037) (← links)
- Initial experiences in the treatment of children with metastatic and recurrent neuroblastoma using meta-iodobenzylguanidine (Q40808227) (← links)
- Membrane Deformability of Erythrocytes with Glucose-6-Phosphate Dehydrogenase Hamburg (Q41233518) (← links)
- Is the IFN-gamma-induced enhancement of superoxide production in CGD-phagocytes caused by increased expression of the p47-phox cytosolic protein (Q41585631) (← links)
- Function of breast milk macrophages (Q41780270) (← links)
- Phagocytosis-associated functions in neonatal monocyte-derived macrophages (Q42011541) (← links)
- Manfred Gahr (Q42087571) (← links)
- Transient oligoarthritis of the lower extremity following influenza B virus infection: Case report (Q42151841) (← links)
- Fetal erythropoiesis and dyserythropoiesis in juvenile chronic myeloid leukaemia (Q43843615) (← links)
- Diseases of the lung and respiratory tract in disorders of immunodeficiency in childhood and adolescence (Q43845136) (← links)
- Phagocytic activities in neonatal monocytes (Q44196788) (← links)
- Persistence of parvovirus B19-DNA in blood of a child with severe combined immunodeficiency associated with chronic pure red cell aplasia (Q44240946) (← links)
- Capofungin therapy for Aspergillus lung infection in a boy with chronic granulomatous disease (Q44338407) (← links)
- Identification of novel GCK and HNF1A/TCF1 mutations and polymorphisms in German families with maturity-onset diabetes of the young (MODY). (Q44387463) (← links)
- Haematemesis and dysphagia in a 20-year-old woman with congenital spine malformation and situs inversus partialis (Q44403911) (← links)
- Wegener's granulomatosis in pediatric patients (Q44437809) (← links)
- Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency in Switzerland. Demonstration of a new variant (G-6-PD Aarau) with chronic nonsphaerocytic haemolytic anaemia (Q44544987) (← links)
- Neonatal septicemia and meningitis in Göttingen, West Germany (Q44653918) (← links)
- Elastase-alpha 1-proteinase inhibitor in early diagnosis of neonatal septicemia (Q44687074) (← links)
- NADPH oxidase is not required for spontaneous and Staphylococcus aureus-induced apoptosis of monocytes (Q44733463) (← links)
- Chronic granulomatous disease (CGD) mimicking neoplasms: a suspected mediastinal teratoma unmasking as thymic granulomas due to X-linked CGD, and 2 related cases (Q44844338) (← links)
- Successful elimination of an invasive Aspergillus nidulans lung infection by voriconazole after failure of a combination of caspofungin and liposomal amphotericin B in a boy with chronic granulomatous disease (Q44934675) (← links)
- Impaired metabolic function of polymorphonuclear leukocytes in glycogen storage disease Ib. (Q45197649) (← links)
- Comparison of different IRT-PAP protocols to screen newborns for cystic fibrosis in three central European populations (Q46081414) (← links)
- Biochemical characterization of a new variant of glucose-6-phosphate dehydrogenase (G-6-PD) deficiency with favism: G-6-PD Bielefeld (author's transl) (Q46102466) (← links)
- Haploinsufficiency, rather than the effect of an excessive production of soluble CD95 (CD95{Delta}TM), is the basis for ALPS Ia in a family with duplicated 3' splice site AG in CD95 intron 5 on one allele (Q46471351) (← links)
- Influence of CARD15 mutations on disease activity and response to therapy in 65 pediatric Crohn patients from Saxony, Germany (Q46577461) (← links)
- A splice-supporting intronic mutation in the last bp position of a cryptic exon within intron 6 of the CYBB gene induces its incorporation into the mRNA causing chronic granulomatous disease (CGD). (Q46974928) (← links)
- The stem cell marker prominin-1/CD133 on membrane particles in human cerebrospinal fluid offers novel approaches for studying central nervous system disease. (Q48014679) (← links)
- Long-term follow-up and outcome of 39 patients with chronic granulomatous disease. (Q50118577) (← links)
- Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus (Q50671884) (← links)
- Five years of experience with biochemical cystic fibrosis newborn screening based on IRT/PAP in Germany. (Q50984178) (← links)
- Triosephosphate isomerase deficiency: haemolytic anaemia, myopathy with altered mitochondria and mental retardation due to a new variant with accelerated enzyme catabolism and diminished specific activity. (Q52048583) (← links)
- [Immunological principles of polysaccharide-protein conjugate vaccination] (Q52061015) (← links)
- Generalised glucosephosphate isomerase (GPI) deficiency causing haemolytic anaemia, neuromuscular symptoms and impairment of granulocytic function: a new syndrome due to a new stable GPI variant with diminished specific activity (GPI Homburg). (Q52081481) (← links)
- Effect of age on homovanillic and 4-hydroxy-3-methoxymandelic acid levels in plasma. (Q53772914) (← links)