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Research 121–150 of 1000+
- [An infant with short stature and red cheeks (Rothmund-Thomson syndrome)].
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Alopecia totalis in an infant
- An Infant with Worsening Rash
- Biotin Deficiency in an Infant Fed with Amino Acid Formula
- Hormones in infant rhesus monkeys’ (Macaca mulatta) hair at birth provide a window into the fetal environment
- Biotin deficiency in an infant fed with amino acid formula and hypoallergenic rice
- White monkey syndrome in infant baboons (Papio species)
- Acrodermatitis dysmetabolica in an infant with maple syrup urine disease
- Association of Infant Physical Development and Rapid Growth With Pubertal Onset Among Girls in Rural China
- Non-invasive biomonitoring of infant exposure to environmental organic pollutants in north-western Spain based on hair analysis. Identification of potential sources
- Tinea Capitis in Infants
- Birth Outcomes of Infants Born to Mothers with Alopecia Areata: A Nationwide Population-based Study in Korea
- A 9-month-old infant with severe scalp dermatosis
- Skin infections among infants and parental awareness: Is there any relationship?
- ALOPECIA AREATA IN INFANTS: IS IT UNCOMMON?
- Kerion Celsi in infants and children—A narrative review 2010–2023
- Disorders of hair in infants and children other than alopecia
- Disorders of pigmentation in infants and children
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Acrodermatitis Enteropathica‐like Eruption in an Infant with Nonketotic Hyperglycinemia
- High Frequency of Symptomatic Zinc Deficiency in Infants in Northern Ethiopia
- A case report of tinea capitis in infant in first year of life
- Deoxycorticosterone’s anticonvulsant effects in infant rats are blocked by finasteride, but not by indomethacin
- Focal Scalp Hair Heterochromia in an Infant
- Kerion caused by Trichophyton tonsurans in an infant
- Multiple Carboxylase Deficiency in an Infant Presenting With Severe Metabolic Acidosis and Sepsis‐Like Features: A Case Report and Literature Review
- Widespread erythematous scaly eruption in an infant with phenylketonuria
- Ring-shaped Alopecia on the Scalp in a 3-month-old Infant
- Unusual Dermatologic Findings in an Extremely Low Birthweight Infant: The Genetic Diagnosis