[Clinical diagnosis of myopathies and neuromyopathies]

[Trans-synaptic retrograde atrophy of the optic nerves: a differential diagnostic problem of expansive intracranial processes].

Srpski arhiv za celokupno lekarstvo·2011

[Hartnup disease (report of 2 cases in one family)].

Srpski arhiv za celokupno lekarstvo·2000

Serum tryptophan to large neutral amino acid ratio and urinary tryptophan in three patients with phenylketonuria in a family. A clinical and biochemical study.

Advances in experimental medicine and biology·2000

[Dysconnection syndrome in a boy with tumorous lesion of corpus callosum].

Srpski arhiv za celokupno lekarstvo·1995

[Progeria syndrome--case report].

Srpski arhiv za celokupno lekarstvo·1994

[Unilateral moyamoya disease associated with acrofacial vitiligo in a 13-year-old patient--case report].

Srpski arhiv za celokupno lekarstvo·1994

A misdiagnosed case of neurinoma of the 8th cranial nerve and adult respiratory distress syndrome.

Neurologija·1990

Electroencephalographic findings in coma caused by fatal chloroquine poisoning.

Neurologija·1990

[Distal latency in motor neuron disease].

Neurologija·1990

Dysplastic granulo-molecular hypertrophy of the cerebellar cortex (L'hermitte-Duclos disease): report of three cases.

Neurologija·1990

Study of serum and cerebrospinal fluid enzymes in diagnosis and differential diagnosis of cerebrovascular diseases.

Neurologija·1990

[A 2-year study of patients up to 55 years of age with cerebrovascular disorders].

Neurologija·1990

A guide to selecting high-performing antibodies for Netrin-1 (UniProt ID: O95631) for use in western blot and immunoprecipitation.

F1000Research·2026

Desmin is not ubiquitously expressed in head and neck muscle fibers.

Journal of anatomy·2026

Advances in Multi-Omics Approaches for Biomarker Identification in Human Rotator Cuff Disease: A Systematic Review.

Journal of orthopaedic research : official publication of the Orthopaedic Research Society·2026

The role of impaired mitochondrial function in neurological manifestations of mitochondrial diseases.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Related Experiment Videos

[Clinical diagnosis of myopathies and neuromyopathies]

Related Concept Videos

[Trans-synaptic retrograde atrophy of the optic nerves: a differential diagnostic problem of expansive intracranial processes].

[Hartnup disease (report of 2 cases in one family)].

Serum tryptophan to large neutral amino acid ratio and urinary tryptophan in three patients with phenylketonuria in a family. A clinical and biochemical study.

[Dysconnection syndrome in a boy with tumorous lesion of corpus callosum].

[Progeria syndrome--case report].

[Unilateral moyamoya disease associated with acrofacial vitiligo in a 13-year-old patient--case report].

A misdiagnosed case of neurinoma of the 8th cranial nerve and adult respiratory distress syndrome.

Electroencephalographic findings in coma caused by fatal chloroquine poisoning.

[Distal latency in motor neuron disease].

Dysplastic granulo-molecular hypertrophy of the cerebellar cortex (L'hermitte-Duclos disease): report of three cases.

Study of serum and cerebrospinal fluid enzymes in diagnosis and differential diagnosis of cerebrovascular diseases.

[A 2-year study of patients up to 55 years of age with cerebrovascular disorders].

A guide to selecting high-performing antibodies for Netrin-1 (UniProt ID: O95631) for use in western blot and immunoprecipitation.

Desmin is not ubiquitously expressed in head and neck muscle fibers.

Advances in Multi-Omics Approaches for Biomarker Identification in Human Rotator Cuff Disease: A Systematic Review.

The role of impaired mitochondrial function in neurological manifestations of mitochondrial diseases.

Related Experiment Videos

[Clinical diagnosis of myopathies and neuromyopathies]

Related Concept Videos

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