Professor, Pediatrics, University of Miami School of Medicine
Pediatric Endocrinology
Dr. Gary D. Berkovitz, MD
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Gary D. Berkovitz, MD practices Pediatric Endocrinology. He went to Perelman School of Medicine at the University of Pennsylvania. He has 2 awards "Regional Top Doctor" and "Super Doctor". Gary D. Berkovitz is a published doctor as well. He has 74 publications published. The latest was: Abnormalities of gonadal differentiation.
Publications
- Madelung-Like Deformity in PseudohypoparaThyroidism Type 1b.
- 46,XX sex reversal With partial duplication of chromosome arm 22q.
- Sex determination, differentiation, and identity.
- Genetic mechanisms that regulate testis determination.
- Characterization of tescalcin, a novel EF-hand protein With a single Ca2+-binding site: metal-binding properties, localization in tissues and cells, and effect on calc...
- 46,XY intersex individuals: phenotypic and etiologic classification, knowledge of condition, and satisfaction With knowledge in adulthood.
- Ambiguous genitalia With perineoscrotal hypospadias in 46,XY individuals: long-term medical, surgical, and psychosexual outcome.
- A nine year old girl With thyrotoxicosis, ataxia, and chorea.
- Expression and evolutionary conservation of the tescalcin gene during development.
- Structural and functional characterization of the mouse tescalcin promoter.
- Attitudes of adult 46, XY intersex persons to clinical management policies.
- Partial gonadal dysgenesis in a patient With a marker Y chromosome.
- Evidence for increased prevalence of SRY mutations in XY females With complete rather than partial gonadal dysgenesis.
- Hypocalcemia in nonwhite breast-fed infants. Vitamin D Deficiency revisited.
- Use of granulosa-luteal cell culture to evaluate low and high clinical responses to menotropin stimulation.
- Abnormalities of gonadal determination and differentiation.
- DNA binding activity of recombinant SRY from normal males and XY females.
- The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditism.
- Induction and superinduction of messenger ribonucleic acid specific for aromatase cytochrome P-450 in cultured human skin fibroblasts.
- Clinical and pathologic spectrum of 46,XY gonadal dysgenesis: its relevance to the understanding of sex differentiation.
- Endocrine evaluation of adults With mild hypospadias.
- Testosterone lowers aromatase activity in cultured human genital skin fibroblasts.
- Abnormal induction of aromatase activity by dexamethasone in fibroblasts from a patient with cortisol resistance.
- Serum 3 alpha-androstanediol glucuronide measurements in sexually mature women with congenital Adrenal hyperplasia during therapy.
- Aromatase activity in microsomal preparations of human genital skin fibroblasts: influence of glucocorticoids.
- Influence of cell culture conditions on aromatase activity in human genital skin fibroblasts.
- Elevation of serum gonadotropins establishes the diagnosis of anorchism in prepubertal boys With bilateral cryptorchidism.
- Androgen receptors in boys With isolated bilateral cryptorchidism.
- Gonadal function in patients with Down Syndrome.
- Gonadal function in men with the Martin-Bell (fragile-X) Syndrome.
- Thyroid function in men with fragile X-linked MR.
- Studies of up-regulation of androgen receptors in genital skin fibroblasts.
- Androgen receptor levels and 5 alpha-reductase activities in preputial skin and chordee tissue of boys With isolated hypospadias.
- Down-regulation of the glucocorticoid receptor by dexamethasone in cultured human skin fibroblasts: implications for the regulation of aromatase activity.
- Factitious transient neonatal hyperthyrotropinemia.
- Aromatase activity in human skin fibroblasts grown in cell culture.
- Effects of 10-(2-propynyl)-estr-4-ene-3,17-dione (MDL 18,962)--a mechanism-based irreversible inhibitor of aromatase--in cultured human foreskin fibroblasts.
- Time-dependent biphasic response of aromatase to dexamethasone in cultured human skin fibroblasts.
- The influence of 4-hydroxy-4-androstene-3,17-dione on androgen metabolism and action in cultured human foreskin fibroblasts.
- Androgen receptor in cultured human Testicular fibroblasts.
- Familial gynecomastia With increased extraglandular aromatization of plasma carbon19-steroids.
- Androgen receptors.
- Etiologic evaluation of male pseudohermaphroditism in infancy and childhood.
- Aromatase activity in cultured human genital skin fibroblasts.
- Gonadal function in two siblings With Fanconi''s anemia.
- Inhibition of 5 alpha-reductase activity and alteration of nuclear testosterone. Dihydrotestosterone ratio in human genital skin fibroblasts.
- Turner Syndrome patients with a ring X chromosome.
- True hermaphroditism.
- Abnormalities of thyroid function and glucose control in subjects with Rett syndrome.
- Assay of plasma testosterone during the first six months of life: importance of chromatographic purification of steroids.
- Combined Leydig cell and Sertoli cell Dysfunction in 46,XX males lacking the sex determining region Y gene.
- Embryonic Testicular regression sequence: a part of the clinical spectrum of 46,XY gonadal dysgenesis.
- Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditism.
- The role of the sex-determining region Y gene in the etiology of 46,XX maleness.
- The effect of epidermal growth factor in human granulosa cells varies With follicle size.
- Report of a kindred With X-linked (or autosomal dominant sex-limited) 46,XY partial gonadal dysgenesis.
- Loss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated With partial testicular determination.
- Mutation analysis of the 2 kb 5'' to SRY in XY females and XY intersex subjects.
- Abnormal gonadal differentiation in two subjects with ambiguous genitalia, Mullerian structures, and normally developed testes: evidence for a defect in gonadal ridge ...
- Linkage analysis of a kindred With inherited 46,XY partial gonadal dysgenesis.
- Analysis of the SRY gene in gonadal tissue of subjects With 46,XY gonadal dysgenesis.
- Nutritional rickets in a child with Down Syndrome.
- Molecular investigation of two male subjects with short stature and a 45,X/46,X,ring(Y) karyoType.
- Evaluation of boys With marked breast development at puberty.
- Growth hormone excess in a child with neurofibromatosis Type 1 and optic pathway tumor: a patient report.
- Abnormalities of gonadal differentiation.
- Prenatal diagnosis of Smith-Lemli-Opitz Syndrome in a pregnancy with low maternal serum oestriol and a sex-reversed fetus.
- Complete androgen insensitivity Syndrome: long-term medical, surgical, and psychosexual outcome.
- Intractable hypoglycemia in a patient with Diabetes mellitus, bilateral nephrectomy, and chronic active hepatitis.
- Tescalcin, a novel gene encoding a putative EF-hand Ca(2+)-binding protein, Col9a3, and renin are expressed in the mouse testis during the early stages of gonadal diff...
- Mutation analysis of subjects With 46, XX sex reversal and 46, XY gonadal dysgenesis does not support the involvement of SOX3 in testis determination.
- Absence of mutations involving the LIM homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis.
- Congenital micropenis: long-term medical, surgical and psychosexual follow-up of individuals raised male or female.
Schools
Perelman School of Medicine University of Pennsylvania
University Of Pittsburgh
Johns Hopkins University School Med
Conditions Treated
- Abnormal Thyroid
- Acromegaly and Gigantism
- Adrenal Insufficiency
- Adrenogenital Disorders
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Doctors Specialties
- Pediatric Endocrinology
Accepted Insurances
Awards
- Regional Top Doctor
- Super Doctor
Education
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Johns Hopkins University -
University of Pittsburgh Medical Center -
Perelman School of Medicine at the University of Pennsylvania
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