Professor, Pediatrics, Medical College of Wisconsin

Pediatric Endocrinology

Patricia Donohoue works in the field of Pediatric Endocrinology. She went to medical school at The Ohio State University College of Medicine. She over the years received 1 awards: "Super Doctor". Patricia Donohoue is a published doctor as well. She has 36 publications published. The latest was: Plasma leptin in diabetic and insulin-treated diabetic and normal rats.

Publications

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• Recognition and Treatment of Concurrent Active and Neurodegenerative Langerhans Cell Histiocytosis: A Case Report.
• Deletion of codons 88-92 of the melanocortin-4 receptor gene: a novel deleterious mutation in an obese female.
• Deep venous thrombosis and Turner Syndrome.
• Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations.
• Phenotypic evolution of classic 21-hydroxylase deficiency.
• Linkage of congenital isolated adrenocorticotropic hormone deficiency to the corticotropin releasing hormone locus using simple sequence repeat polymorphisms.
• E380D: a novel point mutation of CYP21 in an HLA-homozygous patient with salt-losing congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
• Clinical and functional effects of mutations in the DAX-1 gene in patients with adrenal hypoplasia congenita.
• Fasting and leptin modulate adipose and muscle uncoupling protein: divergent effects between messenger ribonucleic acid and protein expression.
• Sympathetic inhibition, leptin, and uncoupling protein subType expression in normal fasting rats.
• Pooling analysis of genetic data: the association of leptin receptor (LEPR) polymorphisms with variables related to human adiposity.
• A meta-analytic investigation of linkage and association of common leptin receptor (LEPR) polymorphisms with body mass index and waist circumference.
• The human complement C4B/steroid 21-hydroxylase (CYP21) and complement C4A/21-hydroxylase pseudogene (CYP21P) intergenic sequences: comparison and identification of po...
• Pituitary gigantism caused by growth hormone excess from infancy.
• Accelerated growth rates in children treated with growth hormone after renal transplantation.
• Congenital adrenal hyperplasia caused by 21-hydroxylase deficiency. Its molecular basis and its remaining therapeutic problems.
• Exon 7 Ncol restriction site within CYP21B (steroid 21-hydroxylase) is a normal polymorphism.
• Glucose tolerance in children with renal allografts and effect of growth hormone treatment.
• Endocrine evaluation of adults with mild hypospadias.
• Two distinct areas of unequal crossingover within the steroid 21-hydroxylase genes produce absence of CYP21B.
• Enhanced growth with growth hormone therapy after renal transplantation.
• Serum 3 alpha-androstanediol glucuronide measurements in sexually mature women with congenital adrenal hyperplasia during therapy.
• Coupling of HLA-A3,Cw6,Bw47,DR7 and a normal CA21HB steroid 21-hydroxylase gene in the Old Order Amish.
• Restriction fragment analysis of duplication of the fourth component of complement (C4A).
• Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein.
• Restriction maps and restriction fragment length polymorphisms of the human 21-hydroxylase genes.
• Congenital adrenal hyperplasia: molecular mechanisms resulting in 21-hydroxylase deficiency.
• Prevalence of polymorphic 21-hydroxylase gene (CA21HB) mutations in salt-losing congenital adrenal hyperplasia.
• A new way to seal glass plates for denaturing gradient gel electrophoresis.
• The HLA-A3, Cw6,B47,DR7 extended haploTypes in salt losing 21-hydroxylase deficiency and in the Old Order Amish: identical class I antigens and class II alleles with a...
• Constitutive human steroid 21-hydroxylase promoter gene and pseudogene activity in steroidogenic and nonsteroidogenic cells with the luciferase gene as a reporter.
• Rat adipose ob mRNA levels in states of altered circulating glucose and insulin.
• Premature sexual development in individuals with neurodevelopmental disabilities.
• Plasma leptin in diabetic and insulin-treated diabetic and normal rats.
• A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutations.

Schools

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• Ohio State University College Of Medcine

• Chldns Hospital

• Rainbow Babies amp Child Hospital

• Johns Hopkins Hospital

Conditions Treated

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• Abnormal Thyroid
• Adrenogenital Disorders
• Craniopharyngioma
• Diabetes Mellitus, Secondary
• View All

Doctors Specialties

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• Pediatric Endocrinology

Accepted Insurances

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Awards

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• Super Doctor

Education

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• Johns Hopkins University
• Case Western Reserve University Affiliated Hospitals
• Ohio State University Hospital
• The Ohio State University College of Medicine

Hospital

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• Children's Hospital of Wisconsin

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