Influence of iodine overloading on neonatal thyroid screening results

Mutational analysis of the PHEX gene: novel point mutations and detection of large deletions by MLPA in patients with X-linked hypophosphatemic rickets.

Calcified tissue international·2009

Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997.

European journal of pediatrics·1999

Newborn screening for hyperphenylalaninemia on day 5: is 240 mumol/liter the most appropriate cut-off level?

Preventive medicine·1990

[The phenylalanine stress test in the classification of patients with phenylketonuria].

Klinische Padiatrie·1989

Interpreting the GnRH stimulation test in girls with central precocious puberty: the role of age and body mass index.

Journal of endocrinological investigation·2026

Lifelong congenital untreated isolated GH deficiency does not alter human leukocyte telomere length.

Journal of endocrinological investigation·2026

Prospective changes in sleep quality and depressive symptom burden following initiation of GLP-1-based therapies in patients with obesity: a real-world study.

Journal of endocrinological investigation·2026

Preimplantation genetic testing for male factor infertility: lights and shadows.

Journal of endocrinological investigation·2026

Functional analysis of 11 CYP21A2 variants reveals greater loss of enzyme activity in cis variants and improves genotype-phenotype correlation in 21-hydroxylase deficiency.

Journal of endocrinological investigation·2026

Functional hyperprolactinemia and subclinical primary hypothyroidism: myth or reality in clinical practice?

Journal of endocrinological investigation·2026

The auditory nerve glial transition zone is a focal site of age-related immune-myelin interactions.

Frontiers in immunology·2026

Profiling complement proteins in pediatric tuberculosis children with or without serological evidence of prior SARS-CoV-2 exposure.

Frontiers in immunology·2026

Collaborative functionality between three types of inflammation in idiopathic pulmonary fibrosis.

Nature immunology·2026

Intraclonal heterogeneity in mature B-cell malignancies: the perspective of immunogenetics.

Seminars in cancer biology·2026

Decoding the spatiotemporal dynamics of T cell immune landscapes in glioblastoma: remodeling precision combination therapies.

Biochimica et biophysica acta. Reviews on cancer·2026

Granular Cell (Granular-type) Fibrous Papule of the Face: Case Report and Literature Review Emphasizing Morphologic and Immunohistochemical Pitfalls.

The American Journal of dermatopathology·2026

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Influence of iodine overloading on neonatal thyroid screening results

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Mutational analysis of the PHEX gene: novel point mutations and detection of large deletions by MLPA in patients with X-linked hypophosphatemic rickets.

Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997.

Newborn screening for hyperphenylalaninemia on day 5: is 240 mumol/liter the most appropriate cut-off level?

[The phenylalanine stress test in the classification of patients with phenylketonuria].

Interpreting the GnRH stimulation test in girls with central precocious puberty: the role of age and body mass index.

Lifelong congenital untreated isolated GH deficiency does not alter human leukocyte telomere length.

Prospective changes in sleep quality and depressive symptom burden following initiation of GLP-1-based therapies in patients with obesity: a real-world study.

Preimplantation genetic testing for male factor infertility: lights and shadows.

Functional analysis of 11 CYP21A2 variants reveals greater loss of enzyme activity in cis variants and improves genotype-phenotype correlation in 21-hydroxylase deficiency.

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Influence of iodine overloading on neonatal thyroid screening results

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