• A case-comparison study of the characteristics of children with a short stature syndrome induced by stress (Hyperphagic Short Stature) and a consecutive series of unaffected "stressed" children
• A rational approach to short stature: focus on use and abuse of growth hormone
• AMINOACIDURIAS IN PATIENTS WITH PSYCHIATRIC DISORDERS AND OTHER RELATED STATES
• Blinded by the UV light: how the focus on transcription-coupled NER has distracted from understanding the mechanisms of Cockayne syndrome neurologic disease
• Clinical aspects, epidemiologic progression of fetal alcoholism: a current daily problem
• Cognitive disorders in children
• Congenital hypothyroidism and neonatal withdrawal syndrome
• DNA repair in neural cells: basic science and clinical implications
• Dysregulation of gene expression as a cause of Cockayne syndrome neurological disease
• Embryopathic alcoholism syndrome (alcoholic embryopathy)
• Folie à deux in the parents of psychosocial dwarfs: two cases
• Food restriction as a form of child abuse in ten cases of psychosocial deprivation dwarfism
• Forensic and family psychiatry in abuse dwarfism: Munchausen's syndrome by proxy, atonement, and addiction to abuse
• Growth of intelligence: failure and catch-up associated respectively with abuse and rescue in the syndrome of abuse dwarfism
• Low birth weight--additional important factor of diagnosis in children with short stature
• Management of Short Stature: Use of Growth Hormone in GH-Deficient and non-GH-Deficient Conditions
• Mania with Aarskog-Scott syndrome
• Munchausen's syndrome by proxy: update
• Nanism caused by water deprivation, with transitory growth hormone deficiency
• Pain agnosia and self-injury in the syndrome of reversible somatotropin deficiency (psychosocial dwarfism)
• Paleodigms and paleodigmatics: a new theoretical construct applicable to Munchausen's syndrome by proxy, child-abuse dwarfism, paraphilias, anorexia nervosa, and other syndromes
• Pediatric emergency medicine: legal briefs
• Psychosocial dwarfism
• Psychosocial dwarfism: psychopathological aspects and putative neuroendocrine markers
• Psychosocial short stature with psychosis: a case report
• Quality of life of growth hormone (GH) deficient young adults during discontinuation and restart of GH therapy
• Quantitation of craniofacial anomalies in utero: fetal alcohol and Crouzon syndromes and thanatophoric dysplasia
• Reversible somatotropin deficiency (psychosocial dwarfism) presenting as conduct disorder and growth hormone deficiency
• Similarities and differences between nonorganic failure to thrive and deprivation dwarfism
• Smith-Lemli-Opitz dwarfism. Report of four cases. Review of the literature
• The beaked, notched, or hooked vertebra: its significance in infants and young children
• The case for 8,5'-cyclopurine-2'-deoxynucleosides as endogenous DNA lesions that cause neurodegeneration in xeroderma pigmentosum
• The past, present, and future of modeling Cockayne Syndrome - A commentary on "Rat Model of Cockayne Syndrome Neurological Disease"
• The syndrome of abuse dwarfism (psychosocial dwarfism or reversible hyposomatotropism)
• Use of growth hormone in the treatment of short stature: boon or abuse?
• Zinc in normal and pathological states
• Zinc metabolism: basic, clinical, and behavioral aspects