Back to Search
ROBERT LINDEMAN, DMD
DMD
General Practice Dentistry
NPI: 1922452994Individual
Specialties, Licenses & Credentials
General Practice DentistryPrimary
Dentist — General Practice
Code: 1223G0001X
32733(TX)
Research & Publications (20)
SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathway.
PMID 19336477·Hum Mol Genet·2009
7-preclinical
Infection outcomes in splenectomized patients with hemoglobinopathies in Australia.
PMID 19136288·Int J Infect Dis·2009
8-other
The maternal-effect gene cellular island encodes aurora B kinase and is essential for furrow formation in the early zebrafish embryo.
PMID 19543364·PLoS Genet·2009
7-preclinical
The role of glycogen synthase kinase-3beta in normal haematopoiesis, angiogenesis and leukaemia.
PMID 18537625·Curr Med Chem·2008
6-review
Glycogen synthase kinase-3beta inhibition preserves hematopoietic stem cell activity and inhibits leukemic cell growth.
PMID 18323411·Stem Cells·2008
7-preclinical
Blood into beta-cells: can adult stem cells be used as a therapy for Type 1 diabetes?
PMID 18154461·Regen Med·2008
6-review
Management and clinical outcomes of transfusion-dependent thalassaemia major in an Australian tertiary referral clinic.
PMID 18205577·Med J Aust·2008
8-other
Recombinant activated factor VII in cardiac surgery: experience from the Australian and New Zealand Haemostasis Registry.
PMID 18291152·Ann Thorac Surg·2008
8-other
Sensitivity of an Acinetobacter baylyi mpl mutant to DNA damage.
PMID 18083886·Appl Environ Microbiol·2008
4-observational
Adherence to desferrioxamine and deferiprone and the impact of deferiprone co-prescription in thalassaemia major patients. Does the addition of deferiprone improve adherence?
PMID 18537970·Br J Haematol·2008
8-other
Hypertension and kidney protection in the elderly: what is the evidence in 2007?
PMID 17487566·Int Urol Nephrol·2007
6-review
The first prenatal diagnosis for veno-occlusive disease and immunodeficiency syndrome, an autosomal recessive condition associated with mutations in SP110.
PMID 17510920·Prenat Diagn·2007
5-case
A screening and intervention program aimed to reduce mortality and serious morbidity associated with severe neonatal alloimmune thrombocytopenia.
PMID 17429009·Blood·2007
3-trial
Rituximab treatment of mild haemophilia A with inhibitors: a proposed treatment protocol.
PMID 17083518·Haemophilia·2006
5-case
Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease.
PMID 16648851·Nat Genet·2006
8-other
Cisplatin inhibition of anthrax lethal toxin.
PMID 16870755·Antimicrob Agents Chemother·2006
4-observational
Analysis of axis induction mutant embryos reveals morphogenetic events associated with zebrafish yolk extension formation.
PMID 16894597·Dev Dyn·2006
7-preclinical
Complex phenotypes in the haemoglobinopathies: recommendations on screening and DNA testing.
PMID 17393977·Pathology·2006
6-review
Seasonal variation of pretransfusion hemoglobin levels in patients with thalassemia major.
PMID 16179377·Blood·2006
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 3 locations total
- Address
- 814 S MILAM ST
FREDERICKSBURG, TX 78624 - Phone
- (830) 872-3033
Quick Facts
- NPI
- 1922452994
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 3
- Publications
- 20
Are you this provider?
Claim Your Profile