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STUART MUMM, MD
MD
Obstetrics & Gynecology Physician
NPI: 1033287131Individual
Specialties, Licenses & Credentials
Obstetrics & Gynecology PhysicianPrimary
Obstetrics & Gynecology
Code: 207V00000X
G35869(CA)AM8525327(CA)
Research & Publications (20)
Effects of polymorphisms of the sex hormone-binding globulin (SHBG) gene on free estradiol and bone mineral density.
PMID 19679209·Bone·2009
8-other
Chronic recurrent multifocal osteomyelitis mimicked in childhood hypophosphatasia.
PMID 19335222·J Bone Miner Res·2009
5-case
The Val432Leu polymorphism of the CYP1B1 gene is associated with differences in estrogen metabolism and bone density.
PMID 18977467·Bone·2009
8-other
Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia.
PMID 18260132·Am J Med Genet A·2008
5-case
WITHDRAWN: Familial Degenerative Encephalopathy with Intracranial Calcification and Metaphyseal Dysplasia.
PMID 19016590·J Bone Miner Res·2008
8-other
Autosomal recessive hypophosphatasia manifesting in utero with long bone deformity but showing spontaneous postnatal improvement.
PMID 18559907·J Clin Endocrinol Metab·2008
5-case
Infantile hypophosphatasia: transplantation therapy trial using bone fragments and cultured osteoblasts.
PMID 17519318·J Clin Endocrinol Metab·2007
5-case
Juvenile Paget's disease: the second reported, oldest patient is homozygous for the TNFRSF11B "Balkan" mutation (966_969delTGACinsCTT), which elevates circulating immunoreactive osteoprotegerin levels.
PMID 17352649·J Bone Miner Res·2007
5-case
Deactivating germline mutations in LEMD3 cause osteopoikilosis and Buschke-Ollendorff syndrome, but not sporadic melorheostosis.
PMID 17087626·J Bone Miner Res·2007
5-case
Sporadic hyperphosphatasia syndrome featuring periostitis and accelerated skeletal turnover without receptor activator of nuclear factor-kappaB, osteoprotegerin, or sequestosome-1 gene defects.
PMID 17284635·J Clin Endocrinol Metab·2007
5-case
Pyridoxine-responsive seizures as the first symptom of infantile hypophosphatasia caused by two novel missense mutations (c.677T>C, p.M226T; c.1112C>T, p.T371I) of the tissue-nonspecific alkaline phosphatase gene.
PMID 17395561·Bone·2007
5-case
Absence of MMP2 mutation in idiopathic multicentric osteolysis with nephropathy.
PMID 17563705·Clin Orthop Relat Res·2007
5-case
Manifestations in a family with autosomal dominant bone fragility and limb-girdle myopathy.
PMID 16419137·Am J Med Genet A·2006
8-other
Homozygosity for TNSALP mutation 1348c>T (Arg433Cys) causes infantile hypophosphatasia manifesting transient disease correction and variably lethal outcome in a kindred of black ancestry.
PMID 16769381·J Pediatr·2006
6-review
Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22: a novel locus for a musculoskeletal syndrome.
PMID 16244874·Hum Genet·2005
8-other
Neonatal lethal osteochondrodysplasia with low serum levels of alkaline phosphatase and osteocalcin.
PMID 15562030·J Clin Endocrinol Metab·2005
5-case
Effect of CYP1A1 gene polymorphisms on estrogen metabolism and bone density.
PMID 15647817·J Bone Miner Res·2005
8-other
Oropharyngeal skeletal disease accompanying high bone mass and novel LRP5 mutation.
PMID 15824861·J Bone Miner Res·2005
5-case
Skeletal changes in epidermal nevus syndrome: does focal bone disease harbor clues concerning pathogenesis?
PMID 16222671·Am J Med Genet A·2005
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1661 SOQUEL DR, SUITE A
SANTA CRUZ, CA 95065 - Phone
- (831) 476-7676
Quick Facts
- NPI
- 1033287131
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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