Physician
Pediatric Endocrinology
Dr. Salman Kirmani, MD
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Salman Kirmani is an expert in the field of Pediatric Endocrinology. He researched medicine at Dow Medical College. Salman Kirmani is a published doctor. He has 30 papers published. The most current publication "Spontaneous coronary artery dissection and its association with heritable connective tissue disorders." Salman Kirmani is registered with Medicare and accepts Medicare payments.
Publications
- Spontaneous coronary artery dissection and its association with heritable connective tissue Disorders.
- Diminished bone strength is observed in adult women and men who sustained a mild trauma distal forearm fracture during childhood.
- Congenital mydriasis and prune belly syndrome in a child with an ACTA2 mutation.
- Novel de novo heterozygous FGFR1 mutation in two siblings with Hartsfield syndrome: A case of gonadal mosaicism.
- Novel De Novo SPOCK1 Mutation in a Proband with Developmental Delay, Microcephaly and Agenesis of Corpus Callosum.
- Fragile X syndrome due to a missense mutation.
- Effects of age on bone mRNA levels of sclerostin and other genes relevant to bone metabolism in humans.
- Effects of Estrogen on Bone mRNA Levels of Sclerostin and Other Genes Relevant to Bone Metabolism in Postmenopausal Women.
- Similarity of geleophysic dysplasia and weill-marchesani syndrome.
- Novel de novo SCN2A Mutation in a Child With Migrating Focal Seizures of Infancy.
- A distal forearm fracture in childhood is associated with an increased risk for future fragility fractures in adult men, but not women.
- Bone strength and structural deficits in children and adolescents with a distal forearm fracture due to mild trauma.
- Septo-optic dysplasia in a patient with an unbalanced 5;12 translocation.
- Response to Cobben et al. "Array CGH on Unstimulated Blood Does Not Detect All Cases of Pallister-Killian Syndrome: Buccal Smear Analysis Should Remain the Diagnostic ...
- Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental Abnormalities.
- "Ocular moyamoya" syndrome in a patient with features of microcephalic osteodysplastic primordial dwarfism type II.
- Chronic tibial nonunion in a Rothmund-Thomson syndrome patient.
- A novel sclerosing skeletal dysplasia with mixed sclerosing bone dysplasia, characteristic syndromic features, and clinical and radiographic evidence of male-male tran...
- Molecular genetic testing in endocrinology - a practical guide.
- Array CGH on unstimulated blood does not detect all cases of Pallister-Killian syndrome: A skin biopsy should remain the diagnostic gold standard.
- Relationship of testosterone and osteocalcin levels during growth.
- Co-morbidity of Sanfilippo Syndrome type C and D: -2-hydroxyglutaric aciduria.
- Transient QT interval prolongation in an infant with Simpson-Golabi-Behmel syndrome.
- Germline TGF-beta receptor mutations and skeletal fragility: a report on two patients with Loeys-Dietz syndrome.
- Towards individualized medicine: insights gained from genomic studies.
- Vitamin A deficiency in an infant with PAGOD syndrome.
- Treatment-resistant meningitis leading to the diagnosis of Currarino syndrome: a case report.
- Bone structure at the distal radius during adolescent growth.
- Phenotypic effects of null and haploInsufficiency of acid-labile subunit in a family with two novel IGFALS gene mutations.
Conditions Treated
- Abnormal Thyroid
- Adrenal Insufficiency
- Adrenogenital Disorders
- Hyperlipidemia
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Doctors Specialties
- Pediatric Endocrinology
Accepted Insurances
Education
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Mayo School of Graduate Medical Education -
Dow Medical College
Hospital
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Mayo Clinic - Rochester, Minnesota
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1487624003 |
| Last Name Of The Provider | KIRMANI |
| First Name Of The Provider | SALMAN |
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