Letter: Unconjugated hyperbilirubinemia in galactosemia

Maternal Phenylketonuria: Long-term Outcomes in Offspring and Post-pregnancy Maternal Characteristics.

JIMD reports·2015

A psychosocial model of a medical problem: Maternal phenylketonuria.

The journal of primary prevention·2013

Newborn Screening for Glutaric Aciduria-II: The New England Experience.

JIMD reports·2013

A limited spectrum of phenylalanine hydroxylase mutations is observed in phenylketonuria patients in western Poland and implications for treatment with 6R tetrahydrobiopterin.

Journal of human genetics·2009

Short-chain acyl-CoA dehydrogenase (SCAD) deficiency: an examination of the medical and neurodevelopmental characteristics of 14 cases identified through newborn screening or clinical symptoms.

Molecular genetics and metabolism·2008

Down syndrome: otolaryngological effects of rapid maxillary expansion.

The Journal of laryngology and otology·2008

Response-Tailored or Standard-Duration Antibiotic Treatment for Infective Endocarditis.

The New England journal of medicine·2026

Aficamten for Symptomatic Nonobstructive Hypertrophic Cardiomyopathy.

The New England journal of medicine·2026

Anticoagulation for Atrial Fibrillation with Intermediate Stroke Risk.

The New England journal of medicine·2026

Eplontersen for Transthyretin Amyloid Cardiomyopathy.

The New England journal of medicine·2026

Myeloproliferative Neoplasms.

The New England journal of medicine·2026

An Atypical Finding in a Patient With Acute Left Flank Pain.

Cureus·2026

A Young Man With Apical Fibrotic Changes on Chest Imaging and History of Pneumothorax.

CHEST pulmonary·2026

Fourteen-year bridge to cure in occult ectopic ACTH syndrome: resection of a 3-mm pulmonary carcinoid.

JCEM case reports·2026

Related Experiment Videos

Letter: Unconjugated hyperbilirubinemia in galactosemia

Related Concept Videos

Maternal Phenylketonuria: Long-term Outcomes in Offspring and Post-pregnancy Maternal Characteristics.

A psychosocial model of a medical problem: Maternal phenylketonuria.

Newborn Screening for Glutaric Aciduria-II: The New England Experience.

A limited spectrum of phenylalanine hydroxylase mutations is observed in phenylketonuria patients in western Poland and implications for treatment with 6R tetrahydrobiopterin.

Short-chain acyl-CoA dehydrogenase (SCAD) deficiency: an examination of the medical and neurodevelopmental characteristics of 14 cases identified through newborn screening or clinical symptoms.

Down syndrome: otolaryngological effects of rapid maxillary expansion.

Response-Tailored or Standard-Duration Antibiotic Treatment for Infective Endocarditis.

Aficamten for Symptomatic Nonobstructive Hypertrophic Cardiomyopathy.

Anticoagulation for Atrial Fibrillation with Intermediate Stroke Risk.

Eplontersen for Transthyretin Amyloid Cardiomyopathy.

Myeloproliferative Neoplasms.

An Atypical Finding in a Patient With Acute Left Flank Pain.

A Young Man With Apical Fibrotic Changes on Chest Imaging and History of Pneumothorax.

Fourteen-year bridge to cure in occult ectopic ACTH syndrome: resection of a 3-mm pulmonary carcinoid.

Large asymptomatic pheochromocytoma with incidental metastatic midgut carcinoid tumor.

Systemic sarcoidosis presenting as asymptomatic hypercalcaemia.

Erratum.

Related Experiment Videos

Letter: Unconjugated hyperbilirubinemia in galactosemia

Related Concept Videos

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