Physician

Pediatric Endocrinology

Dr. Maya B. Lodish, MD

Maya Lodish works in the field of Pediatric Endocrinology. She went to Yale University School of Medicine. Yale University School of Medicine is a one of the best medicals schools. Yale University School of Medicine is ranked 7/57 in Research/PrimaryCare. Maya Lodish is also published. She has 42 publications published. The lastest publication: "A genetic and molecular update on adrenocortical causes of Cushing syndrome.'

Publications

A genetic and molecular update on adrenocortical causes of Cushing syndrome.
Pituitary gigantism: update on molecular biology and management.
Endocrine disorders in fanconi anemia: recommendations for screening and treatment.
Primary Aldosteronism and ARMC5 variants.
Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in human and mice.
Germline PRKACA amplification leads to Cushing syndrome caused by 3 adrenocortical pathologic phenotypes.
Post-operative growth is different in various forms of pediatric Cushing's syndrome.
Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation.
A gender-dependent analysis of Cushing's disease in childhood: pre- and post-operative follow-up.
Ectopic ACTH and CRH co-secreting tumors in children and adolescents causing Cushing syndrome: a diagnostic enigma and how to solve it.
Not All Glucocorticoid-Induced Obesity is the Same: Differences in Adiposity Among Various Diagnostic Groups of Cushing Syndrome.
Use of Aromatase Inhibitors in Large Cell Calcifying Sertoli Cell Tumors: Effects on Gynecomastia, Growth Velocity, and Bone Age.
Vitamin B12 deficiency in an adolescent girl with polycystic ovarian syndrome.
Racial disparities in pubertal development.
Vandetanib in Children and Adolescents with Multiple Endocrine Neoplasia Type 2B Associated Medullary Thyroid Carcinoma.
Kinase inhibitors: adverse effects related to the endocrine system.
Identification of novel genetic variants in phosphodiesterase 8B (PDE8B), a cAMP-specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort of pati...
The differential diagnosis of familial lentiginosis syndromes.
SDHB immunohistochemistry: a useful tool in the diagnosis of Carney-Stratakis and Carney triad gastrointestinal stromal tumors.
Rare and unusual endocrine cancer syndromes with mutated genes.
Effects of Cushing disease on bone mineral density in a pediatric population.
Blood pressure in pediatric patients with Cushing syndrome.
Extensive and largely reversible ischemic cerebral infarctions in a prepubertal child with hypertension and Cushing disease.
Insulinoma and gastrinoma syndromes from a single intrapancreatic neuroendocrine tumor.
GATA-factor dependence of the multitype zinc-finger protein FOG-1 for its essential role in megakaryopoiesis.
Metastatic pheochromocytoma/paraganglioma related to primary tumor development in childhood or adolescence: significant link to SDHB mutations.
The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with geneti...
111In-Octreotide Scintigraphy for Identification of Metastatic Medullary Thyroid Carcinoma in Children and Adolescents.
An Intronic mutation is associated with prolactinoma in a young boy, decreased penetrance in his large family, and variable effects on MEN1 mRNA and protein.
Reversible posterior encephalopathy syndrome associated with micronodular adrenocortical disease and Cushing syndrome.
Pseudotumor cerebri after surgical remission of Cushing's disease.
The growth hormone receptor (GHR) polymorphism in growth-retarded children with Cushing disease: lack of association with growth and measures of the somatotropic axis.
Frequent phosphodiesterase 11A gene (PDE11A) defects in patients with Carney complex (CNC) caused by PRKAR1A mutations: PDE11A may contribute to adrenal and testicular...
Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations.
Proper coronary vascular development and heart morphogenesis depend on interaction of GATA-4 with FOG cofactors.
Use of altered specificity mutants to probe a specific protein-protein interaction in differentiation: the GATA-1:FOG complex.
RET oncogene in MEN2, MEN2B, MTC and other forms of thyroid cancer.
Succinate dehydrogenase gene mutations are strongly associated with paraganglioma of the organ of Zuckerkandl.
Intrauterine growth retardation associated with precocious puberty and sertoli cell hyperplasia.
Endocrine tumours in neurofibromatosis type 1, tuberous sclerosis and related syndromes.
Endocrine side effects of broad-acting kinase inhibitors.

Schools

Yale University
Johns Hopkins Hospital
National Institutes Of Health

Doctors Specialties

Pediatric Endocrinology

Accepted Insurances

Education

National Institutes of Health Clinical Center
Johns Hopkins University
Yale University School of Medicine

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