Assistant Professor, Pediatrics, University of Texas Southwestern Medical Center

Pediatric Nephrology

Dr. Matthias T. Wolf is an expert in the field of Pediatric Nephrology. He studied medicine at University of Texas Southwestern Medical School. Matthias Wolf is a published doctor. He published 30 publications, including: 'Ten novel mutations found in Aniridia.'

Publications

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• Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal Cystic disease to the function of primary cilia and left-right axis determination.
• Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis.
• The ciliary gene RPGRIP1L is mutated in cerebello-oculo-Renal syndrome (Joubert syndrome type B) and Meckel syndrome.
• Evidence of oligogenic inheritance in nephronophthisis.
• Mutational analysis of the RPGRIP1L gene in patients with Joubert Syndrome and nephronophthisis.
• The Uromodulin C744G mutation causes MCKD2 and FJHN in children and adults and may be due to a possible founder effect.
• Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).
• A new missense mutation of the vasopressin-neurophysin II gene in a family with neurohypophyseal diabetes insipidus.
• A gene locus for branchio-otic Syndrome maps to chromosome 14q21.3-q24.3.
• Ten novel mutations found in Aniridia.
• Refinement of the critical region for MCKD1 by detection of transcontinental haplotype sharing.
• Follow-up of five patients with FHHNC due to mutations in the Paracellin-1 gene.
• A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution.
• Pulmonary re-occurrence of post-transplant lymphoproliferative Disease with hypogammaglobulinaemia.
• A gene locus for steroid-resistant Nephrotic syndrome with deafness maps to chromosome 14q24.2.
• Mutations of the Uromodulin gene in MCKD type 2 patients cluster in exon 4, which encodes three EGF-like domains.
• Telomeric refinement of the MCKD1 locus on chromosome 1q21.
• Medullary cystic Kidney disease type 1 in a large Native-American kindred.
• Expression and phenotype analysis of the nephrocystin-1 and nephrocystin-4 homologs in Caenorhabditis elegans.
• Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2-q34.2 by total genome search for linkage.
• Medullary cystic Kidney disease type 1: mutational analysis in 37 genes based on haplotype sharing.
• Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencing.
• Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT).
• A systematic approach to mapping recessive Disease genes in individuals from outbred populations.
• Uromodulin is expressed in Renal primary cilia and UMOD mutations result in decreased ciliary uromodulin expression.
• Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy.
• Nephronophthisis.
• Mutation analysis of 18 nephronophthisis associated ciliopathy Disease genes using a DNA pooling and next generation sequencing strategy.
• Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD.

Procedures Preformed

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• Hemodialysis
• Peritoneal Dialysis

Conditions Treated

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• Acidosis
• Acute Kidney Failure
• Calcium Metabolism Disorders
• Chronic Glomerulonephritis
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Doctors Specialties

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• Pediatric Nephrology

Accepted Insurances

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• Aetna HMO
• Choice Plus POS II
• Blue Card PPO
• Blue Choice
• Cigna HMO
• Cigna PPO
• Great West Healthcare-Cigna PPO
• LocalPlus
• Open Access Plus
• First Health (Coventry Health Care) PPO
• Preferred PPO
• PHCS Network PPO
• Choice Plus POS
• Navigate HMO
• Navigate POS
• Options PPO

Education

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• University of Texas Southwestern Medical School
• Ludwig Maximilian University of Munich Faculty of Medicine

Hospital

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• University of Texas Southwestern Medical Center

Helpful Reviews

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Medicare Facts

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National Provider Identifier [NPI]	1407059090
Last Name Of The Provider	WOLF
First Name Of The Provider	MATTHIAS
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