Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The role of clinical pharmacology in molecular genetics.

International journal of clinical pharmacology and therapeutics - 1 Apr 1997

Robertson D

Abstract excerpt

PROBLEM: Discovering the causes of unusual phenotypes in human subjects is an important aspect of patient-oriented research. MATERIAL: The tools of clinical pharmacology are uniquely useful in addressing these problems. PATIENTS, SUBJECTS, OR CASE HISTORIES: We evaluated a 42-year-old patient with lifelong orthostatic hypotension and ptosis of the eyelids. He underwent a series of biochemical, physiological, and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Blood Pressure
Share to Dopamine
Share to Dopamine beta-Hydroxylase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Neurons

Share to Norepinephrine

Share to Phenotype

Share to Sympathetic Nervous System

Share to Synaptic Transmission

Source

Identifiers

PMID: 9112133

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The role of clinical pharmacology in molecular genetics.PMID 9112133Read ↗

Genetic basis of clinical catecholamine disorders.Semantic proximity Read ↗

Genetics and molecular biology of hypotension.Semantic proximity Read ↗

[From gene to disease; dopamine-beta-hydroxylase deficiency and orthostatic hypotension].Semantic proximity Read ↗

Genetic basis of autonomic dysfunction.Semantic proximity Read ↗

Catecholamine phenotyping: clues to the diagnosis, treatment, and pathophysiology of neurogenetic disorders.Semantic proximity Read ↗

Congenital absence of norepinephrine due to CYB561 mutations.Semantic proximity Read ↗

Human genetics of plasma dopamine beta-hydroxylase activity: applications to research in psychiatry and neurology.Semantic proximity Read ↗

Dopamine beta-hydroxylase deficiency.Semantic proximity Read ↗

Dopamine beta‐hydroxylase and its genetic variants in human health and diseaseSemantic proximity Read ↗

Human phenotypes and animal knockout models of genetic autonomic disorders.Semantic proximity Read ↗

Dihydropteridine reductase deficiency in man: from biology to treatment.Semantic proximity Read ↗

De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: a genomics approach to personalized medicine.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.