Myelin deficiency in hereditary pituitary dwarfism: a biochemical and morphological study.

Morphological study of a hereditary rat cataract.

Abnormalities of tooth development in pituitary dwarfism.

Acid maltase deficiency in adults. Clinical, morphological and biochemical study of three patients.

Pituitary dwarfism in German Shepherd dogs.

Morphological and biochemical characterization of light and heavy myelin isolated from developing rat brain.

Biochemical, morphological, and functional aspects of systemic and local vitamin A deficiency in the respiratory tract.

Ragged-red fibers. A biochemical and morphological study.

Carnitine deficiency: clinical, morphological, and biochemical observations in a fatal case.

Low setting of feedback regulation of TSH secretion by thyroxine in pituitary dwarfism with TSH-releasing hormone deficiency.

Pituitary dwarfism in Saarloos and Czechoslovakian wolfdogs is associated with a mutation in LHX3.

[A study of anti-pituitary-antibodies in patients with hypopituitarism and their hereditary background].

Dental Abnormalities in Pituitary Dwarfism: A Case Report and Review of the Literature.

Lubricin expression in human osteoarthritic knee meniscus and synovial fluid: a morphological, immunohistochemical and biochemical study.

Myelinogenesis in optic nerve. A morphological, autoradiographic, and biochemical analysis.

Biochemical and clinical features of hereditary hyperprolinemia.

Biochemical and pathological studies of myelin in hexachlorophene intoxication.

The development of hepatic drug-metabolizing enzymes in perinatal guinea pigs: a biochemical and morphological study.

Myelination of brain in experimental hypothyroidism. An electron-microscopic and biochemical study of purified myelin isolates.

Myelin deficiency (md): a neurologic mutant in the Wistar rat.

Hereditary chondrodystrophy in the rabbit. Genetics and pathology of a new mutant, a model for metatropic dwarfism.

[Hereditary heterozygote factor VII deficiency].

Neuromyopathy and restrictive cardiomyopathy with accumulation of intermediate filaments: a clinical, morphological and biochemical study.

Clinical, biochemical, and morphological correlates in patients bearing growth hormone-secreting pituitary tumors with or without constitutively active adenylyl cyclase.

Hereditary respiration deficiency in Saccharomycodes ludwigii.

Suggest Documents

Morphological study of a hereditary rat cataract.

Abnormalities of tooth development in pituitary dwarfism.

Acid maltase deficiency in adults. Clinical, morphological and biochemical study of three patients.

Pituitary dwarfism in German Shepherd dogs.

Morphological and biochemical characterization of light and heavy myelin isolated from developing rat brain.

Biochemical, morphological, and functional aspects of systemic and local vitamin A deficiency in the respiratory tract.

Ragged-red fibers. A biochemical and morphological study.

Carnitine deficiency: clinical, morphological, and biochemical observations in a fatal case.

Low setting of feedback regulation of TSH secretion by thyroxine in pituitary dwarfism with TSH-releasing hormone deficiency.

Pituitary dwarfism in Saarloos and Czechoslovakian wolfdogs is associated with a mutation in LHX3.

[A study of anti-pituitary-antibodies in patients with hypopituitarism and their hereditary background].

Dental Abnormalities in Pituitary Dwarfism: A Case Report and Review of the Literature.

Lubricin expression in human osteoarthritic knee meniscus and synovial fluid: a morphological, immunohistochemical and biochemical study.

Myelinogenesis in optic nerve. A morphological, autoradiographic, and biochemical analysis.

Biochemical and clinical features of hereditary hyperprolinemia.

Biochemical and pathological studies of myelin in hexachlorophene intoxication.

The development of hepatic drug-metabolizing enzymes in perinatal guinea pigs: a biochemical and morphological study.

Myelination of brain in experimental hypothyroidism. An electron-microscopic and biochemical study of purified myelin isolates.

Myelin deficiency (md): a neurologic mutant in the Wistar rat.

Hereditary chondrodystrophy in the rabbit. Genetics and pathology of a new mutant, a model for metatropic dwarfism.

[Hereditary heterozygote factor VII deficiency].

Neuromyopathy and restrictive cardiomyopathy with accumulation of intermediate filaments: a clinical, morphological and biochemical study.

Clinical, biochemical, and morphological correlates in patients bearing growth hormone-secreting pituitary tumors with or without constitutively active adenylyl cyclase.

Hereditary respiration deficiency in Saccharomycodes ludwigii.

Myelin deficiency in hereditary pituitary dwarfism: a biochemical and morphological study.

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