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Your search keyword '"Garagorri, J."' showing total 7 results
Start Over Author "Garagorri, J." Journal anales espanoles de pediatria
7 results on '"Garagorri, J."'

1. [Endocrinologic changes in obesity].

Author

Bueno M, Sarriá A, Legido A, Garagorri JM, González I, Bueno G, and Bueno-Lozano M

Subjects
Adipose Tissue anatomy & histology, Child, Circadian Rhythm, Female, Health Status, Humans, Hydrocortisone blood, Hypothalamo-Hypophyseal System metabolism, Insulin blood, Male, Obesity blood, Endocrine Glands physiopathology, Obesity physiopathology
Published
1993

2. [Growth deficiency: dignostic methodology].

Author

Garagorri JM

Subjects
Adolescent, Adult, Child, Child, Preschool, Chromosome Aberrations genetics, Female, Fetal Growth Retardation diagnosis, Growth Disorders classification, Growth Disorders etiology, Growth Disorders genetics, Growth Hormone biosynthesis, Growth Hormone metabolism, Growth Substances metabolism, Humans, Male, Nutrition Disorders complications, Reference Values, Secretory Rate, Sex Factors, Body Height, Growth physiology, Growth Disorders diagnosis, Growth Hormone deficiency
Published
1992

3. [Growth retardation and diseases with a late manifestation].

Author

Garagorri JM, Bueno M, Lázaro A, and Cortés N

Subjects
Adolescent, Asthma complications, Chronic Disease, Female, Growth Disorders physiopathology, Humans, Kidney Diseases complications, Male, Nutritional Physiological Phenomena, Time Factors, Turner Syndrome complications, Growth Disorders etiology
Published
1991

4. [Tricho-rhino-phalangeal dysplasia type I (Giedion's syndrome) (author's transl)].

Author

Bueno M, Garagorri J, Sanz J, Sarriá A, Vega ML, and Seral F

Subjects
Adolescent, Adult, Cartilage pathology, Chondrodysplasia Punctata pathology, Dermatoglyphics, Diagnosis, Differential, Female, Humans, Male, Pedigree, Chondrodysplasia Punctata genetics
Abstract

A new case of these rare entity is described. Histopathology and ultrastructure of cartilage is studied pointing out some pathogenics aspects.

Published
1979

7. [Shwachman's syndrome: pancreatic exocrine insufficiency retarded growth, metaphyseal dysostosis and neutropenia (author's transl)].

Author

Sarriá A, Lázaro A, Lázaro J, Garagorri J, Sanz J, and Bueno M

Subjects
Biopsy, Bone Resorption diagnosis, Child, Dwarfism diagnosis, Fibrous Dysplasia of Bone diagnosis, Gait, Humans, Male, Neutropenia diagnosis, Pancreatic Diseases diagnosis, Syndrome, Bone Diseases diagnosis, Reflex, Abnormal diagnosis
Abstract

A boy of 5 8/12 years of age affected with Shwachman's Syndrome is presented. He showed frequent respiratory infections that can be in order with a low account in T-lymphocytes found on immunological study. A cytoplasmic degenerative process was found after microscopical and ultrastructural vision of osteoid tissue, which is compatible with biochemical alterations.

Published
1977

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