Angel F. Berio MD PA General Practice

Family Medicine

Angel Berio practices Family Medicine. He went to medical school at University of Puerto Rico School of Medicine. He received 1 awards: "Meaningful Use Stage 1 Certification". Doctor Angel F. Berio, MD is a published doctor as well. He has 101 publications published. The latest was: Prophylaxis of cystine calculi by low dose of alpha-mercapto-propionyl-glycine administered every other day. He accepts all Medicare patients.

Publications

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• [Arachnoid cyst, hypoplasic temporal lobe and facial anomalies: a neurocristopathy].
• Kearns-Sayre syndrome with corneal dystrophy, hypomagnesemia, GH deficiency, and reduced visual acuity.
• [Serious cerebral malformations (corpus callosum aplasia, prosencephalic cyst), internal carotid canal and facial malformations due to neural crest abnormalities, asso...
• Kearns-Sayre sindrome with hypomagnesemia and cardiac block.
• Craniofacial abnormalities in a patient with cytochrome-c-oxidase deficiency subsequently developing Kearns-Sayre syndrome.
• [Leigh syndrome with facial abnormalities: a neurocristopathy].
• Three cases of Kearns-Sayre syndrome with cardiac blocks.
• Facial anomalies in a patient with cytochrome-oxidase deficiency and subsequent Kearns-Sayre syndrome with growth hormone deficiency.
• Kearns-Sayre syndrome, compensated hypothyroidism and complete atrio-ventricular block.
• [Kearns-Sayre syndrome].
• A case of Kearns-Sayre sindrome with autoimmune thyroiditis and complete atrio-ventricular block.
• Enhanced biofilm-production in pathogens isolated from patients with rare metabolic disorders.
• Facial anomalies in patients with cytochrome-c-oxidase (COX) deficiency: a dysneurulation.
• [Kearns-Sayre syndrome associated with growth hormone deficiency].
• [Stickler syndrome: maxillo-facial abnormalities].
• [FAMILIAL LACTOSE INTOLERANCE].
• PROBLEMS REGARDING INTESTINAL ABSORPTION OF MONOSACCHARIDES. THE 3-METHYL-O-GLUCOSE TEST.
• SIX CASES OF LACTOSE INTOLERANCE. LACTOSE INTOLERANCE AND COELIAC DISEASE. DISACCHARIDASES ACTIVITY IN THE INTESTINAL MUCOSA ASCERTAINED WITH THE PERORAL BIOPSY.
• [CONGENITAL MALFORMATIONS OF THE CENTRAL NERVOUS SYSTEM IN THE CASE REPORTS OF THE ISTITUTO "GASLINI" FROM 1939 TO 1962 (CLINICO-STATISTICAL FINDINGS)].
• DISACCHARIDE INTOLERANCE AND MUCOVISCIDOSIS.
• [Maxillo-facial abnormalities in Kearns-Sayre syndrome].
• A case of Kearns-Sayre syndrome with autoimmune thyroiditis and possible Hashimoto encephalopathy.
• Prophylaxia of cystine calculosis by alpha-mercaptopropionyl-glycine administered continuously or every other day.
• Kearns-Sayre syndrome associated with de Toni-Debré-Fanconi syndrome due to cytochrome-c-oxidase (COX) deficiency.
• [Kearns-Sayre syndrome with GH deficiency].
• Prophylaxis of cystine calculi by low dose of alpha-mercapto-propionyl-glycine administered every other day.
• [Medical and surgical therapy of familial hypophosphatemic vitamin D resistant rickets with ambulation disorders].
• [Marinesco-Sjögren syndrome with chronic progressive ophthalmoplegia caused by presumed defective oxidative phosphorylation].
• [A case of chronic progressive external ophthalmoplegia with severe scoliosis].
• [Primary Toni-Debré-Fanconi syndrome].
• [The Kearns-Sayre syndrome].
• Improvement of Kearns-Sayre syndrome with controlled carbohydrate intake and coenzyme Q10 therapy.
• [Progressive chronic external ophthalmoplegia. Personal experience].
• [Prolonged diet therapy in a case of homocystinuria].
• [The Toni-Caffey-Silverman syndrome. Personal experience].
• [Physiologic and paraphysiologic aminoacidurias revealed by high pressure electrophoresis followed by solvent chromatography].
• [Pathology of the isthmus faucium and adjacent structures in childhood].
• [On the dental changes during various pediatric diseases].
• [Cystinuria. A personal case series].
• [Evaluation of body components in chronic renal failure].
• [Electrophoretic and electrophoretic-chromatographic pictures in homocystinuria].
• [Monodimensional electrophoretic picture of the most frequent hyperaminoacidurias caused by disorders of the intermediate metabolism of aminoacids (pre-renal)].
• [Prevention of cysteine calculosis by the continuous administration of alpha-mercaptopropionylglycine].
• [Electrophoretic and electrophoretic-chromatographic picture in diseases of defective renal transport of amino acids with particular reference to personal cases].
• [Disorders of dental calcification in untreated and treated vitamin D-resistant rickets].
• Disaccharidase activities of duodenal mucosa in children. (Normal subjects, coeliac DISEASE, malnutrition, cystic fibrosis of pancreas, other chronic enteropathies).
• [Nodular hyperplasia of the liver in children].
• [Polyepiphyseal dysplasia with peripheral localization (Léri-Silfverskiöld type). Description of a case].
• [Congenital malformations of the digestive tract. Case records of the Istituto G. Gaslini from 1939 to 1963].
• Lactase deficiency in de Toni-Debré-Fanconi Syndrome. Relationship between lactase activity and calcium absorption.
• Relationships between lactase activity and calcium absorption. Lactose intolerance in hyperparathyroidism.
• Dietotherapy by means of vegetable (soya bean) milk in infants with chronic and transitory intolerance of cow''s milk.
• [Congenital malformations of the urinary apparatus. (Clinico-statistical study done on cases of the Istituto "Gaslini" from 1939 to 1963)].
• [Gluten intolerance. Cases from the Clinica Pediatrica of Genoa].
• [The 3-methylglucose test in the diagnosis of intetinal absorption of carbohydrates].
• [Considerations on some cases of chronic diarrhea not due to gluten intolerance].
• [Duodenal biopsy in the child].
• [Disaccharidase activity of the duodenl mucosa in the normal child. Technics of determination].
• [Disaccharidase activity of the duodenamucosa in gluten intolerance, in pancreatic cystic fibrosis and in malnutrition].
• [The Sturge-Weber disease: complete and incomplete forms (contribution of 5 cases)].
• [Neurogenic muscular atrophies of childhood. Case records of the Clinica Pediatrica "G. Gaslini" of Genoa from 1959 to 1967].
• [Personal experience with chromatographic methods of demonstrating aminated substances (amino acids and amines)].
• Lactase activity in experimental rickets and vitamin D intoxication.
• [Statistical considerations on the incidence of congenital malformations at the Instituto "Gaslini"].
• [Dwarfism (primordial?) with congenital renal hypoplasia and (idiopathic) De Toni-Debré-Fanconi syndrome].
• [Hypervitaminosis D. Comments of 12 cases observed between 1959 and 1966 at the Genova pediatric clinic].
• [Considerations on antitussive treatments in pediatrics: The use of a new compound: medazonamide].
• [Studies of the origin of urinary amines in children].
• [High-tension electrophoresis associated with ascending chromatography in the detection of amino acid disorders. Personal experience].
• [Fecal elimination of amines in normal and pathological conditions].
• [Effect on serum lipids and body growth of a special type of milk with partial replacement of lipids by vegetable fats].
• [Amino acid metabolism disorders in infancy with special reference to phenylketonuria. 3. General problems of diseases of aminoacid transport and metabolism. Personal ...
• [Study on the fecal excretion of aminoacids by means of monodimensional high-voltage electrophoresis. Results of personal studies].
• [Personal results in screening amino acid diseases by means of the method of Scriver et al].
• [Further research in the field of extraction and demonstration of amines in biological materials].
• [Lumbar pneumoencephalography in the diagnosis of cerebrospinal abnormalities in children].
• [On 2 uncommon cases of cardio-muscular glycogenosis (with enzyme study)].
• [On 3 cases of glycogenosis with predominantly hepatic symptoms (type 1 b, type VI or type VII o Hers?, type III)].
• [On a case of leucinosis treated with a low-leucine diet].
• [The use of some recent methods for diagnosis of aminoacidopathy. Personal results].
• [Studies of inborn errors of amino acid metabolism and urinary excretion of -phenylethylamine, using screening methods].
• [Spondylo-epiphyseal dysplasias. Nosological considerations on 2 rare forms: Silfverskiold''s disease and the Morquio-like form of polyepiphysial dysplasia].
• [Poly-epiphysial dysplasia with extensive involvement of the spine. Apropos of a case polyepiphysial dysplasia comparable, in some characteristics, to Norquio''s disea...
• [The Toni-Caffey-Silverman syndrome. Observation of a case with isolated involvement of the mandible].
• [Diseases of altered amino acid metabolism].
• [Diseases caused by altered intermediate metabolism of amino acids].
• [Favorable results with an association of L-dopa and amantadine added to penicillamine in the treatment of Wilson''s disease].
• [Demonstration urinary amines by means of 2-dimensional chromatography. Personal results in children with various physiopathological conditions].
• Results with screening methods in an investigation of aminoacid metabolism disturbances and urinary excretion of beta-phenylethylamines.
• [Prophylaxis of caries and other dental anomalies in the child].
• A case of de Toni-Caffey''s syndrome with isolated involvement of the mandible.
• [Case of Caffey''s syndrome with changes limited to the mandible].
• [Data on therapy of Syndenham''s chorea. Case records of the Clinica Pediatrica of Geno during the period 1955-1966].
• [Recent acquisitions on neurogenic amyotrophy in the pediatric age. Description of a case of early juvenile neurogenic amyotrophy (Graveleau type?)].
• [Aminuria in children. Studies in infantile cerebropathies].
• [Long-term personal experience in the diagnosis of amino acidopathies by chromatography of serum according to the method of Scriver et al].
• [Prophylaxis of cystinic calculosis with alpha mercapto propionylglycine. Personal cases].
• [Results of diet treatment of a new case of homocystinuria diagnosed late].
• [A monodimensional electrophoretic picture of urinary amino acids in de Toni-Debré-Fanconi syndrome caused by cystinosis].
• [A further contribution to our knowledge of cystinuria diagnosed by high-voltage electrophoresis].

Schools

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• University Of Puerto Rico School Of Medicine

• St Vincent39s Hospital and Medical Center

• Jackson MemorialUniversity Of Miami

Doctors Specialties

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• Family Medicine

Accepted Insurances

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• Aetna HMO
• Choice Plus POS II
• Cigna HMO
• Cigna PPO
• Great West Healthcare-Cigna PPO
• Open Access Plus
• Choice Care PPO
• Select HMO
• Choice Plus POS
• Navigate HMO
• Navigate POS
• Options PPO

Awards

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• Meaningful Use Stage 1 Certification

Education

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• Jackson Memorial Hospital - Jackson Health System
• University of Puerto Rico School of Medicine

Drug Facts

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NPI NUMBER		1225094675
NPPES Provider LastName		BERIO
NPPES Provider FirstName		ANGEL
NPPES Provider ZIPCode		331265541
NPPES Provider State		FL
Specialty Description		General Practice
Total Claim Count		13659.0
Distinct Opioid Count		2.0
Opioid Claim Count		165.0
Percent Opioid Claims		1.21

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Medicare Facts

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National Provider Identifier [NPI]	1225094675
Last Name Of The Provider	BERIO
First Name Of The Provider	ANGEL
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