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Alfonso M Martinez is currently accepting new patients!
Alfonso M Martinez, MD
Alfonso M Martinez,
CHILDREN'S HOSPITAL OF WISCONSIN SINCE 1996
Children's Hospital of Wisconsin-Main Campus
8915 W. Connell Ave
(877) 607-5280 (appointment)
Areas of Interest
Education & Awards
1979, Universidad Autonoma (De Guadalajera, Mexico), MD
1993, Cincinnati Children's Hospital Medical Center
1985, Michigan State University (East Lansing, MI)
1981, Universidad Autonoma (De Guadalajera, Mexico)
1988, Universidad Autonoma (De Guadalajera, Mexico)
1996, Cincinnati Children's Hospital Medical Center
Research & Publications
Risk of advanced proximal neoplasms according to distal colorectal findings: comparison of sigmoidoscopy-based strategies.
Modifiable endoscopic factors that influence the adenoma detection rate in colorectal cancer screening colonoscopies.
Clinical audit of COPD patients requiring hospital admissions in Spain: AUDIPOC study.
Identifying youth nonadherence in clinical settings: data-based recommendations for children and adolescents with inflammatory bowel disease.
Experimental demonstration of subcarrier multiplexed quantum key distribution system.
Colonoscopy versus fecal immunochemical testing in colorectal-cancer screening.
Prevalence of heart failure with preserved ejection fraction in Latin American, Middle Eastern, and North African Regions in the I PREFER study (Identification of Patients With Heart Failure and PREserved Systolic Function: an epidemiological regional study).
Herpesvirus active replication in multiple sclerosis: a genetic control?
Safety of percutaneous endoscopic gastrostomy in medically complicated infants.
The factors affecting the distribution of babesiosis in dogs in Poland.
CD46 in a Spanish cohort of multiple sclerosis patients: genetics, mRNA expression and response to interferon-beta treatment.
[Primary rhinopharyngeal tuberculosis: an unusual location].
Effect of ezetimibe-simvastatine over endothelial dysfunction in dyslipidemic patients: assessment by 13N-ammonia positron emission tomography.
Kinematic characteristics of myositis ossificans of the semimembranosus muscle in a dog.
Evidence of epistasis between TNFRSF14 and TNFRSF6B polymorphisms in patients with rheumatoid arthritis.
NO role of NOS2A susceptibility polymorphisms in rheumatoid arthritis.
Localization of Type 1 Diabetes susceptibility in the ancestral haplotype 18.2 by high density SNP mapping.
Role of ATG16L1 Thr300Ala polymorphism in inflammatory bowel disease: a Study in the Spanish population and a meta-analysis.
Novel association of the interleukin 2-interleukin 21 region with inflammatory bowel disease.
Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15(-) Crohn's disease patients.
Suggested association of NOS2A polymorphism in idiopathic achalasia: no evidence in a large case-control study.
6q23 polymorphisms in rheumatoid arthritis Spanish patients.
The IL6-174G/C polymorphism is associated with celiac disease susceptibility in girls.
[Prevalence of left ventricular hypertrophy, atrial fibrillation and cardiovascular disease in hypertensive patients of Andalusia, Spain. PREHVIA study].
Listeria monocytogenes infection in patients with rheumatic diseases on TNF-alpha antagonist therapy: the Spanish Study Group experience.
Endothelial dysfunction in recently diagnosed type 2 diabetic patients evaluated by PET.
ICAM1 R241 is not associated with celiac disease in the Spanish population.
Polymorphisms in the selenoprotein S gene: lack of association with autoimmune inflammatory diseases.
Interleukin-6 gene variation in Spanish patients with immunoglobulin-A deficiency.
IL23R and IL12B polymorphisms in Spanish IBD patients: no evidence of interaction.
Association of MYO9B haplotype with type 1 diabetes.
IFIH1-GCA-KCNH7 locus: influence on multiple sclerosis risk.
CD209 in inflammatory bowel disease: a case-control study in the Spanish population.
IL4 in the 5q31 context: association studies of type 1 diabetes and rheumatoid arthritis in the Spanish population.
TLR4 haplotypes in multiple sclerosis: a case-control study in the Spanish population.
Gender-specific association of the PTPN22 C1858T polymorphism with achalasia.
Influence of the inducible nitric oxide synthase gene (NOS2A) on inflammatory bowel disease susceptibility.
Macrophage migration inhibitory factor gene: influence on rheumatoid arthritis susceptibility.
Role of the PXR gene locus in inflammatory bowel diseases.
Identification of peptide inhibitors of transforming growth factor beta 1 using a phage-displayed peptide library.
Strong protective effect of DR3 against ulcerative colitis in the Spanish population.
Susceptibility to type 1 diabetes conferred by the PTPN22 C1858T polymorphism in the Spanish population.
Environment-gene interaction in multiple sclerosis: human herpesvirus 6 and MHC2TA.
E. coli multiresistant meningitis after transrectal prostate biopsy.
FcRL3 and multiple sclerosis pathogenesis: role in autoimmunity?
Surveillance and antimicrobial resistance of Salmonella strains isolated from slaughtered pigs in Spain.
Role of the MHC2TA gene in autoimmune diseases.
Interleukin-10 polymorphisms in Spanish IgA deficiency patients: a case-control and family study.
Evidence for the association of the SLC22A4 and SLC22A5 genes with type 1 diabetes: a case control study.
Genetic markers linked to rheumatoid arthritis are also strongly associated with articular manifestations in ulcerative colitis patients.
Role of SLC22A4, SLC22A5, and RUNX1 genes in rheumatoid arthritis.
Interleukin-10 haplotypes in Celiac Disease in the Spanish population.
A functional PTPN22 polymorphism associated with several autoimmune diseases is not associated with IgA deficiency in the Spanish population.
Polymorphisms in interleukin-10 gene according to mutations of NOD2/CARD15 gene and relation to phenotype in Spanish patients with Crohn's disease.
MDR1 gene: susceptibility in Spanish Crohn's disease and ulcerative colitis patients.
Association of the organic cation transporter OCTN genes with Crohn's disease in the Spanish population.
Early B-cell Factor gene association with multiple sclerosis in the Spanish population.
Th1 cytokine polymorphisms in spanish patients with type 1 diabetes.
Role of interleukin 4 in Spanish multiple sclerosis patients.
A recombined haplotype in the major histocompatibility region contains a cluster of genes conferring high susceptibility to ulcerative colitis in the Spanish population.
Improving the quantification of highly overlapping chromatographic peaks by using product unit neural networks modeled by an evolutionary algorithm.
Interleukin-10 polymorphisms in Spanish patients with IBD.
Type 1 diabetes in the Spanish population: additional factors to class II HLA-DR3 and -DR4.
Unilateral pleural effusions associated with stenoses of left brachiocephalic veins in haemodialysis patients.
IBD5 polymorphisms in inflammatory bowel disease: association with response to infliximab.
Osteopontin gene polymorphisms in Spanish patients with rheumatoid arthritis.
IBD1 and IBD3 determine location of Crohn's disease in the Spanish population.
Association of the major histocompatibility complex with response to infliximab therapy in rheumatoid arthritis patients.
Epidemiologic and clinical characteristics of children with newly diagnosed inflammatory bowel disease in Wisconsin: a statewide population-based study.
Optical microwave filter based on spectral slicing by use of arrayed waveguide gratings.
Microwave photonic filters with negative coefficients based on phase inversion in an electro-optic modulator.
Arrayed waveguide Sagnac interferometer.
Full distortion induced by dispersion evaluation and optical bandwidth constraining of fiber Bragg grating demultiplexers over analogue SCM systems.
MHC susceptibility genes to IgA deficiency are located in different regions on different HLA haplotypes.
Spontaneous improvement of the renal function in a patient with HIV-associated focal glomerulosclerosis.
Infliximab retreatment in adults and children with Crohn's disease: risk factors for the development of delayed severe systemic reaction.
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