Debbie Schugg
Social Worker
124 RIVER RD SALINAS CA, 93908About
Debbie Schugg Other is a top Social Worker in SALINAS, CA. With a passion for the field and an unwavering commitment to their specialty, Debbie Schugg Other is an expert in changing the lives of their patients for the better. Through their designated cause and expertise in the field, Debbie Schugg Other is a prime example of a true leader in health care. As a leader and expert in their field, Debbie Schugg Other is passionate about enhancing patient quality of life. They embody the values of communication, safety, and trust when dealing directly with patients. In SALINAS, CA, Debbie Schugg Other is a true asset to their field and dedicated to the profession of medicine.
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Expert Publications
Data provided by the National Library of Medicine- The Kniest syndrome.
- A lysosomal storage disease with severe dwarfism, severe joint contractures, mild-moderate mental retardation, corneal opacities and retinal abnormalities.
- A recessive form of congenital scoliosis different from spondylothoracic dysplasia.
- International classification of osteochondrodysplasias. International Working Group on Constitutional Diseases of Bone.
- THE RADIOGRAPHIC MANIFESTATIONS OF THE HS-MUCOPOLYSACCHARIDOSIS OF SANFILIPPO, WITH DISCUSSION OF THIS CONDITION IN RELATION TO THE OTHER MUCOPOLYSACCHARIDOSES AND A CLASSIFICATION OF THESE FUNDAMENTALLY SIMILAR ENTITIES.
- SPONDYLOEPIPHYSIAL DYSPLASIA TARDA. HEREDITARY CHONDRODYSPLASIA WITH CHARACTERISTIC VERTEBRAL CONFIGURATION IN THE ADULT.
- DIASTROPHIC DWARFISM IN EARLY INFANCY.
- DYSCHONDROSTEOSIS, A HEREDITABLE BONE DYSPLASIA WITH CHARACTERISTIC ROENTGENOGRAPHIC FEATURES.
- ROENTGEN FINDINGS OF INCREASED INTRACRANIAL PRESSURE AND COMMUNICATING HYDROCEPHALUS AS INSIDIOUS MANIFESTATIONS OF CHRONIC HISTIOCYTOSIS-X.
- Dominant mesomelic dysplasia, ankle, carpal, and tarsal synostosis type: a new autosomal dominant bone disorder.
- Short rib syndrome Beemer-Langer type with polydactyly: a multiple congenital anomalies syndrome.
- A severe autosomal recessive acromesomelic dysplasia, the Hunter-Thompson type, and comparison with the Grebe type.
- Thanatophoric dysplasia and cloverleaf skull.
- Increasing frequency of a syndrome of multiple osseous defects?
- Spondyloepiphyseal dysplasia.
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