Dr. Jesse J Pitt MD
OB-GYN (Obstetrician-Gynecologist)
2825 Fort Missoula Road Suite 225 Missoula MT, 59804About
Dr. Jesse Pitt is an obstetrician-gynecologist practicing in Missoula, MT. Dr. Pitt specializes in women's health, particularly the female reproductive system, pregnancy and childbirth. As an obstetrician-gynecologist, or OB-GYN, Dr. Pitt can treat a number of health issues related to the vagina, uterus, ovaries, fallopian tubes and breasts. Dr Pitt can also treat women during pregnancy, labor, childbirth and the postpartum period. In this specialty, doctors focus on reproductive care from puberty through adulthood.
Education and Training
Wayne State Univ Sch of Med, Detroit Mi 1970
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Pitfalls in the use of 2-octynoic acid as an in vivo model of medium-chain acyl-coenzyme A dehydrogenase deficiency: ketone turnover and metabolite studies in the rat.
- Fasting medium chain acyl-coenzyme A dehydrogenase--deficient children can make ketones.
- Pseudo-glutarylcarnitinaemia in medium-chain acyl-CoA dehydrogenase deficiency detected by tandem mass spectrometry newborn screening.
- VLCAD deficiency: pitfalls in newborn screening and confirmation of diagnosis by mutation analysis.
- Gas chromatographic-mass spectrometric characterisation of unsaturated dicarboxylic acids in urine.
- Atypical pyroglutamic aciduria: possible role of paracetamol.
- Episodes of severe metabolic acidosis in a patient with 3-methylglutaconic aciduria.
- Striatal degeneration in glutaric acidaemia type II.
- Effect of fructose on delirium tremens.
- Trimethylaminuria, fish odour syndrome: a new method of detection and response to treatment with metronidazole.
- Excretion of 3,6-epoxydicarboxylic acids in peroxisomal disorders.
- Novel glycine conjugates in medium-chain acyl-CoA dehydrogenase deficiency.
- In vivo disposal of phenylalanine in phenylketonuria: a study of two siblings.
- Succinic semialdehyde dehydrogenase deficiency: low excretion of metabolites in a neonate.
- Fasting hypoketotic coma in a child with deficiency of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase.
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