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Atypical Post-Injection Reactions with Delayed Onset Following Glatiramer Acetate 40 mg: Need for Titration?

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Occurrence of thanatophoric dysplasia type I (R248C) and hypochondroplasia (N540K) mutations in two patients with achondroplasia phenotype.

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Clinical dysmorphology·2001

Congenital hypertrichosis, cardiomegaly, and osteochondrodysplasia (Cantú syndrome): a new case with unusual radiological findings.

American journal of medical genetics·2000

Phenotypic comparison of an osteogenesis imperfecta type IV proband with a de novo alpha2(I) Gly922 --> Ser substitution in type I collagen and an unrelated patient with an identical mutation.

Biochemical and molecular medicine·1998

A Cys634Gly substitution of the RET proto-oncogene in a family with recurrence of multiple endocrine neoplasia type 2A and cutaneous lichen amyloidosis.

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Pathologica·2026

Metastatic melanoma with heterologous bone after neoadjuvant immunotherapy: diagnostic insights.

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Technical feasibility of a long read, fourth generation sequencing platform in diagnostic profiling of clinical routine samples: a proof-of-concept study.

Pathologica·2026

Toward a positive psychology-informed framework for environmental law, human flourishing, and ecological citizenship.

Frontiers in psychology·2026

Ecological harm and criminal thresholds: A pilot legal-ecological coding framework for environmental crime judgments.

Open research Europe·2026

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Wiener medizinische Wochenschrift (1946)·2026

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EFSA journal. European Food Safety Authority·2026

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EFSA journal. European Food Safety Authority·2026

Ethical Considerations for Wastewater and Environmental Surveillance in Carceral Settings: Building a Framework to Guide Public Health Interventions.

American journal of public health·2026

Related Experiment Videos

[Camurati-Engelmann disease. Description of 2 related cases. Therapeutic approach with peridural anesthesia]

Related Concept Videos

Atypical Post-Injection Reactions with Delayed Onset Following Glatiramer Acetate 40 mg: Need for Titration?

Occurrence of thanatophoric dysplasia type I (R248C) and hypochondroplasia (N540K) mutations in two patients with achondroplasia phenotype.

Brachyphalangy, feet polydactyly, absent/hypoplastic tibiae: a further case and review of main diagnostic findings.

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Phenotypic comparison of an osteogenesis imperfecta type IV proband with a de novo alpha2(I) Gly922 --> Ser substitution in type I collagen and an unrelated patient with an identical mutation.

A Cys634Gly substitution of the RET proto-oncogene in a family with recurrence of multiple endocrine neoplasia type 2A and cutaneous lichen amyloidosis.

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