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Publications by Thais R. Villela
[PROVISIONAL] Growth Hormone Insensitivity (Laron Syndrome): Report of a New Family and Review of Brazilian Patients
Genetics and Molecular Biology
Genetics
Molecular Biology
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A Mammalian Model for Laron Syndrome Produced by Targeted Disruption of the Mouse Growth Hormone Receptor/Binding Protein Gene (The Laron Mouse)
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
A Novel Mutation of Exon 7 in Growth Hormone Receptor mRNA in a Patient With Growth Hormone Insensitivity Syndrome and Neurofibromatosis Type I
International Journal of Molecular Medicine
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The Insulin-Likegrowth Factor-1 (Igf I) Gene Is Expressed in Skin Fibroblasts From Children With Laron Growth Hormone (Gh) Insensitivity
Pediatric Research
Child Health
Pediatrics
Perinatology
Pfeiffer Syndrome: Report of a Family and Review of the Literature.
Journal of Medical Genetics
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The D152H Mutation Found in Growth Hormone Insensitivity Syndrome Impairs Expression and Function of Human Growth Hormone Receptor but Is Silent in Rat Receptor
Journal of Molecular Endocrinology
Endocrinology
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Partial Androgen Insensitivity Syndrome – Case Report
Pediatric Endocrinology
Report of a Large Brazilian Family With a Very Attenuated Form of Hunter Syndrome (MPS II)
JIMD Reports
Internal Medicine
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Molecular Biology
Biochemistry
Endocrinology
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Diabetes
