Medical Director, Johns Hopkins USA
Medical Genetics
George Sack, MD works in the field of Medical Genetics. He researched medicine at Johns Hopkins University School of Medicine. Johns Hopkins University School of Medicine is a one of the best medicals schools. Johns Hopkins University School of Medicine has a rank of 3 in research and a 29 in primary care He received 1 awards: "Whos Who in Medicine and Healthcare". George Sack has written publications. He has 59 publications published with PubMed. The lastest publication is: 'A fusion protein between serum amyloid A and staphylococcal nuclease--synthesis, purification, and structural studies.'
Publications
- [The behavior of EEG following pneumoencephalography].
- Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients.
- Mutational analysis of patients with X-linked adrenoleukodystrophy.
- Serum amyloid A and P protein genes in familial Mediterranean fever.
- Serum amyloid A (SAA) gene variations in familial Mediterranean fever.
- Frequent alterations of visual pigment genes in adrenoleukodystrophy.
- Linkage of adrenoleukodystrophy to a polymorphic DNA probe.
- Color vision defects in adrenomyeloneuropathy.
- Molecular analysis of the human serum amyloid A (SAA) gene family.
- The human serum amyloid A (SAA)-encoding gene GSAA1: nucleotide sequence and possible autocrine-collagenase-inducer function.
- Acute intermittent porphyria.
- Hereditary canine spinal muscular atrophy: canine motor neuron disease.
- Highly polymorphic domains of the human serum amyloid A (SAA) gene GSAA1.
- Exclusion of linkage between familial Mediterranean fever and the human serum amyloid A (SAA) gene cluster.
- The human serum amyloid A locus SAA4 is a pseudogene.
- Serum amyloid A gene transcription in synovial cells during retroviral arthritis.
- Familial amyloidosis, Finnish type: G654----a mutation of the gelsolin gene in Finnish families and an unrelated American family.
- Trousseau''s syndrome and other manifestations of chronic disseminated coagulopathy in patients with neoplasms: clinical, pathophysiologic, and therapeutic features.
- A dominantly inherited form of arthrogryposis multiplex congenita with unusual dermatoglyphics.
- Gastric acidity in cholera and noncholera diarrhoea.
- A souble 17 beta-hydroxysteroid dehydrogenase from human placenta. The binding of pyridine nucleotides and steroids.
- Use of restriction endonucleases in analyzing the genome of simian virus 40.
- Characterization of "heavy" and "light" SV40-like particles from a patient with PML.
- Studies of simian virus 40 DNA. VII. A cleavage map of the SV40 genome.
- Studies of SV40 DNA. VI. Cleavage of SV40 DNA by restriction endonuclease from Hemophilus parainfluenzae.
- The nucleic acid of an SV40-like virus isolated from a patient with progressive multifocal leukoencephalopathy.
- Linear skin atrophy, scarring alopecia, anonychia, and tongue lesion: a "new" syndrome?
- Infection and prematurity as the cause of linear skin atrophy, alopecia, anonychia, and tongue lesions?
- Genetics clinics of The Johns Hopkins Hospital. Surgical intervention in achondroplasia. Cervical and lumbar laminectomy for spinal stenosis in achondroplasia.
- Clinical diversity in Gaucher's disease.
- Three forms of dominant amyloid neuropathy.
- Autosomal dominant inheritance of hereditary canine spinal muscular atrophy.
- Arthrogryposis multiplex congenita occurring with maternal multiple sclerosis.
- Malignant complications of neurofibromatosis.
- Molecular cloning of human genes for serum amyloid A.
- Human cell transformation by simian virus 40. Biologic features of cloned lines.
- Human cell transformation by simian virus 40--a review.
- Unusual cardiac, renal and pulmonary involvement in Gaucher''s disease. Intersitial glucocerebroside accumulation, pulmonary hypertension and fatal bone marrow emboliz...
- Adrenoleukodystrophy: overlapping deletions point to a gene location in Xq28.
- Chromosomal rearrangement segregating with adrenoleukodystrophy: associated changes in color vision.
- Chromosomal rearrangement segregating with adrenoleukodystrophy: a molecular analysis.
- Visual pigment gene changes in adrenoleukodystrophy.
- Cleft palate with autosomal recessive transmission in Brittany spaniels.
- What is the role of molecular genetics in modern veterinary practice?
- Thoracolumbosacral laminectomy in achondroplasia: long-term results in 22 patients.
- Molecular biologic approaches to prenatal defects.
- Expression of serum amyloid A genes in mouse brain: unprecedented response to inflammatory mediators.
- A fusion protein between serum amyloid A and staphylococcal nuclease--synthesis, purification, and structural studies.
- Diagnostic molecular genetics.
- Canine genetic linkage study using heterologous DNA probes.
- Introduction to the minireviews series on mitochondrial matters in amyotrophic lateral sclerosis, Lou Gehrig’s disease.
- Introduction to the mini-review series on mitochondrial matters in epilepsy.
- Mitochondrial matters in Huntington disease.
- Mitochondrial matters in Parkinson disease: introduction.
- Comprehensive outpatient health assessment: a case-finding tool in 500 consecutive asymptomatic individuals.
- Hyperphosphatasia with massive osteoectasia: a 45-year follow-up.
- Plaque formation and purification of BK virus in cultured human urinary cells.
- Familial spastic paraplegia-clinical and pathologic studies in a large kindred.
Schools
Johns Hopkins University School Of Medicine
Johns Hopkins University Osler Med
Johns Hopkins
Doctors Specialties
- Clinical Genetics
- Medical Genetics
Accepted Insurances
Awards
- Whos Who in Medicine and Healthcare
Education
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Johns Hopkins University
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Johns Hopkins University School of Medicine
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