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2. An interesting question of Pompe disease. A case report

Author

Accomando, S., Montaperto, D., Fragapane, M. L., Amato, G. M., Corsello, G., Francesco Cappello, Maresi, E., ACCOMANDO, S, MONTAPERTO, D, FRAGAPANE, ML, AMATO, GM, CORSELLO, G, CAPPELLO, F, and MARESI, E

Subjects
Pompe Disease, Liver, Glycogen Storage Disease Type II, Humans, Infant, Glycogen, Glycogen storage disease, Glycogen storage disease type II, Female, Children
Abstract

Glycogenosis type II or Pompe disease is an inherited autosomal recessive disorder known in 3 different clinical forms (infantile, juvenile and adult). We report on a case diagnosed as a classic infantile form with the worst outcome of all 3 described, if we had followed and executed a correct and complete diagnostic pathway. A 7 months old female child was admitted for fever and dyspnoea. At chest auscultation weepings and weezings were found; on the cardiac apex a murmur due to mitralic failure was retrieved. The thorax X-ray showed a greatly increased heart shadow with a cardiothoracic index of 0.75. ECG showed high voltages and signs of bilateral ventricular hypertrophy. Cardiac ultrasonography confirmed the presence of a big heart with an enormous swollen left ventricle and a severe mitralic failure. The clinical diagnosis of infantile Pompe disease was confirmed by the almost total absence of cellular acid a-glucosidase activity but we couldn't perform the assay because of the rapid exitus of our patient, which occurred before glycogen storage disease II was suspected. So, we tried to compare our case with others reported in the literature in order to ratify our diagnostic hypothesis. The contribution of genetic counseling practiced on all the couples at risk remains useful every time that a certain diagnosis is made.

Published
2006

3. Familial Protein Losing Enteropathy

Author

ACCOMANDO, Salvatore, ALBINO, Claudia Accursia, CORSELLO, Giovanni, Acierno, C, RAPPA, Francesca, Fragapane, M. L, Montaperto, D, Amato, G. M, Accomando, S, Acierno, C, Rappa, F, Albino, C, Fragapane, M.L, Montaperto, D, Amato, G.M, and Corsello, G

Subjects
Settore MED/38 - Pediatria Generale E Specialistica, PLE, Lymphangectasia
Published
2006

4. Utilità degli ASCA nel follow up della malattia di Crohn

Author

ACCOMANDO, Salvatore, ALBINO, Claudia Accursia, CORSELLO, Giovanni, Montaperto, D, Fragapane, M. L, Amato, G. M, Accomando, S, Montaperto, D, Fragapane, M.L, Albino, C, Amato, G.M, and Corsello

Subjects
Settore MED/38 - Pediatria Generale E Specialistica, MICI
Published
2005

6. Intolleranza al latte: nuovo algoritmo diagnostico

Author

ACCOMANDO, Salvatore, ALBINO, Claudia Accursia, CORSELLO, Giovanni, Montaperto, D, Fragapane, M. L, Serraino, F, Amato, G. M, Benigno, V, Accomando, S, Albino, C, Montaperto, D, Fragapane, M.L, Serraino, F, Amato, G.M, Benigno, V, and Corsello, G

Subjects
APLV, Settore MED/38 - Pediatria Generale E Specialistica
Published
2005

8. Discitis in childhood: Integrated neuroradiological imaging in diagnosis and follow-up of one case

Author

Giuffre M., Amato G. M., Manfre L., Morello A., Giuffre M., Amato G.M., Manfre L., and Morello A.

Subjects
Discitis, Magnetic resonance imaging, Child
Abstract

Discitis is an inflammatory disease of the intervertebral disc which has usually a benign evolution in childhood. It often recognizes an infectious etiology. Still discussed however is the possibility of a primitive discal involvement (not secondary to a vertebral inflammation) or of a non infectious etiology and the subsequent more correct diagnostic-therapeutic procedures. We report a case of a girl with discitis diagnosed early and treated with antibiotics and orthopedic corset, whose follow-up shows a benign evolution. We underline the importance of modern neuroradiological imaging: in particular, MR plays a major role in the inflammatory diseases of the column, both in diagnosis and in follow-up. MR scans of the involved disc allow frequent controls without radiogenic risks and with a good resolution because of the multiplanarity typical of the method.

Published
1997

9. Use of intravenous immunoglobulins in Lyell syndrome: Experience of three cases

Author

Giuffre M., Carta M., Amato G. M., Giuffre M., Carta M., and Amato G.M.

Subjects
Lyell syndrome, Intravenous Immunoglobulines (IVIG), Toxic Epidermal Necrolysis (TEN)
Abstract

We present our experience of treatment of the last three cases of Lyell syndrome we have observed. They are three female children, aged between 16 months and 3 years, who showed many features in common with severely burnt patients (large exuding lesions, severe reduction of circulating plasmatic volume, large denuded body surfaces, severe tendency to infections, ...). Therefore, together with the already known scheme of treatment (corticosteroids, correction of hydroelectrolitic balance, antimicrobials), we decided to use intravenous Immunoglobulins (IVIG), which had been already positively used in severely burnt patients. The favorable evolution of the affection in all three cases and the absence of any complications, above all infectious, sproned us to refer our experience.

Published
1996

10. Prevalence and distribution of Inflammatory Bowel Diseases in a group of immigrant children. Is Inflammatory Bowel Diseases incidence increasing also in children coming from developing countries?

Author

Salvatore ACCOMANDO, Caserta, M., Fragapane, M. L., Cataldo, F., Carlucci, A., Baldassarre, M., Intini, A. C., Corvaglia, L., Masi, M., Spina, M., Bombace, V., Lodin, D., Gentile, T., Montesanti, M., Corona, G., Galizzi, R., Bonarrigo, A., Cassone, R., Sferlazzas, C., Magazzù, G., Prampolini, L., Fredella, C., Frison, E., Pitter, M., Amarri, S., Balli, F., Zaffaroni, M., Oderda, G., Bona, G., Greco, P., Amato, G. M., Angelis, G. L., Bizzarri, B., Fornalori, F., Ughi, C., Zanacca, C., Castro, M., Diamanti, A., Ferretti, F., Papadatou, B., Gambara, M., Bonamico, M., Guida, M., Fusco, P., and Musumeci, S.

11. The Quality of Life of Children and Adolescents with X-Linked Agammaglobulinemia

Author

Soresina A., Nacinovich R., Bomba M., Cassani M., Molinaro A., Sciotto A., Martino S., Cardinale F., De Mattia D., Putti C., Dellepiane R.M., Felici L., Parrinello G., Neri F., Plebani A., Pierani P., DeMattia D., Martire B., Armenio L., Dammacco F., Ranieri G., Masi M., Miniaci A., Pession A., Rondelli R., Notarangelo L. D., Cao, Cossu F., Del Giacco S., Manconi P., Evangelista I., Magro S., Morgione S., STRISCIUGLIO, PIETRO, Anastasio E., Schillirò G., Paganelli R., Sticca M., Sperlì D., Carpino L., Bernini G., Azzari C., Maggi E., Romagnani S., Matucci A., Vultaggio A., Castagnola E., Gattorno M., Presta G., Civino A., Gambaretto G., Fasoli S., Salpietro C., Pietrogrande M.C., DellePiane R.M., Panisi C., Cambiaghi G., Pietrogrande M., Roncarolo M.G., Aiuti A., Masera G., Biondi A., Sala A., PIGNATA, CLAUDIO, Poggi V., Menna G., Di Nardo R., D'Apuzzo A., Pelliccia A., Correra A., Marone G., SPADARO, GIUSEPPE, Carli M., Zanesco L., Basso G., Putti M.C., Semenzato G., Agostini C., Amato G.M., Aricò M., Trizzino A., Izzi G., Bertolini P., Locatelli F., Zecca M., Rondini G., Marseglia G.L., Maccario R., Bossi G., Favre C., Consolini R., Vecchi V., Sacchini P., Rinaldi G., Ugazio A.G., Rossi P., Livadiotti S., Cancrini C., Finocchi A., Stabile A., Duse M., Iacobini M., Quinti I., Moschese V., Cecere F., Morgese G., Acquaviva A., De Zan G., Strafella S., Tamaro P., Rabusin M., Tovo P.A., Nespoli L., Marinoni M., Porcellini A., Cazzola G.A., Annarosa, Soresina, Renata, Nacinovich, Monica, Bomba, Morena, Cassani, Molinaro, Anna, Antonella, Sciotto, Silvana, Martino, Fabio, Cardinale, Domenico, Mattia, Caterina, Putti, Rosa Maria, Dellepiane, Leonardo, Felici, Giovanni, Parrinello, Francesca, Neri, Alessandro, Plebani, Soresina, A, Nacinovich, R, Bomba, M, Cassani, M, Molinaro, A, Sciotto, A, Martino, S, Cardinale, F, De Mattia, D, Putti, C, Dellepiane, R, Felici, L, Parrinello, G, Neri, F, Plebani, A, Soresina, A., Nacinovich, R., Bomba, M., Cassani, M., Molinaro, A., Sciotto, A., Martino, S., Cardinale, F., De Mattia, D., Putti, C., Dellepiane, R. M., Felici, L., Parrinello, G., Neri, F., Plebani, A., Pierani, P., Demattia, D., Martire, B., Armenio, L., Dammacco, F., Ranieri, G., Masi, M., Miniaci, A., Pession, A., Rondelli, R., Notarangelo, L. D., Cao, Cossu, F., Del Giacco, S., Manconi, P., Evangelista, I., Magro, S., Morgione, S., Strisciuglio, Pietro, Anastasio, E., Schillirò, G., Paganelli, R., Sticca, M., Sperlì, D., Carpino, L., Bernini, G., Azzari, C., Maggi, E., Romagnani, S., Matucci, A., Vultaggio, A., Castagnola, E., Gattorno, M., Presta, G., Civino, A., Gambaretto, G., Fasoli, S., Salpietro, C., Pietrogrande, M. C., Panisi, C., Cambiaghi, G., Pietrogrande, M., Roncarolo, M. G., Aiuti, A., Masera, G., Biondi, A., Sala, A., Pignata, Claudio, Poggi, V., Menna, G., Di Nardo, R., D'Apuzzo, A., Pelliccia, A., Correra, A., Marone, G., Spadaro, Giuseppe, Carli, M., Zanesco, L., Basso, G., Putti, M. C., Semenzato, G., Agostini, C., Amato, G. M., Aricò, M., Trizzino, A., Izzi, G., Bertolini, P., Locatelli, F., Zecca, M., Rondini, G., Marseglia, G. L., Maccario, R., Bossi, G., Favre, C., Consolini, R., Vecchi, V., Sacchini, P., Rinaldi, G., Ugazio, A. G., Rossi, P., Livadiotti, S., Cancrini, C., Finocchi, A., Stabile, A., Duse, M., Iacobini, M., Quinti, I., Moschese, V., Cecere, F., Morgese, G., Acquaviva, A., De Zan, G., Strafella, S., Tamaro, P., Rabusin, M., Tovo, P. A., Nespoli, L., Marinoni, M., Porcellini, A., and Cazzola, G. A.

Subjects
Male, Pediatrics, medicine.medical_specialty, x-linked agammaglobulinemia, Activities of daily living, Adolescent, X-linked agammaglobulinemia, Health Status, Immunology, pedsql 4.0 generic core scale, Quality of life, children, Agammaglobulinemia, Surveys and Questionnaires, Activities of Daily Living, health-related quality of life, parents, medicine, Humans, Immunology and Allergy, PedsQL 4.0 Generic Core Scale, Child, Settore MED/38 - Pediatria Generale e Specialistica, Health related quality of life, quality of live, business.industry, Immunoglobulins, Intravenous, Genetic Diseases, X-Linked, medicine.disease, Socioeconomic Factors, Child, Preschool, Mutation, Quality of Life, Female, X-linked agammaglobulinemia - children - parents - health-related quality of life - PedsQL 4.0 Generic Core Scale, business
Abstract

Introduction: The health-related quality of life in X-linked agammaglobulinemia was investigated in 25 children and adolescents patients through the Italian version of Pediatric Quality of Life Inventory 4.0 Generic Core Scale for patients aged less then 18 years, comparing child perception to that of the parents and the physician's evaluation. The data were compared with the ones of 80 healthy controls and the literature data of a group of patients with rheumatic diseases. Discussion: The agammaglobulinemia subjects perceived a lower global quality of life than the healthy subjects, but significantly higher than the rheumatic diseases controls. The clinical relevance of health-related quality of life assessment in X-linked agammaglobulinemia pediatric patients is discussed. © 2008 Springer Science+Business Media, LLC.

Published
2009

12. Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study

Author

Plebani, A, Soresina, A, Rondelli, R, Amato, Gm, Azzari, C, Cardinale, F, Cazzola, G, Consolini, R, De Mattia, D, Dell'Erba, G, Duse, M, Fiorini, M, Martino, Silvana, Martire, B, Masi, M, Monafo, V, Moschese, V, Notarangelo, Ld, Orlandi, P, Panei, P, Pession, A, Pietrogrande, Mc, Pignata, C, Quinti, I, Ragno, V, Rossi, P, Sciotto, A, Stabile, A, Italian Pediatric Group for XLA AIEOP, Plebani, A., Soresina, A., Rondelli, R., Amato, G. M., Azzari, C., Cardinale, F., Cazzola, G., Consolini, R., DE MATTIA, D., Dell'Erba, G., Duse, M., Fiorini, M., Martino, S., Martire, B., Masi, M., Monafo, V., Moschese, V., Notarangelo, L. D., Orlandi, P., Panei, P., Pession, A., Pietrogrande, M. C., Pignata, Claudio, Quinti, I., Ragno, V., Rossi, P., Sciotto, A., and Stabile, A.

Subjects
Lung Diseases, Adult, Male, Pediatrics, medicine.medical_specialty, Genetic Linkage, Agammaglobulinemia, Humans, Infant, Newborn, Protein-Tyrosine Kinases, Child, Child, Preschool, X Chromosome, Immunoglobulins, Intravenous, Cohort Studies, Chronic Disease, Follow-Up Studies, Adolescent, Mutation, clinical features, X-linked agammaglobulinemia, Immunology, Immunoglobulins, infections, intravenous immunoglobulin, BTK mutation, Sepsis, Immunopathology, Epidemiology, medicine, Agammaglobulinaemia Tyrosine Kinase, Immunology and Allergy, Preschool, Settore MED/38 - Pediatria Generale e Specialistica, BTK mutations, business.industry, Chronic sinusitis, Meningoencephalitis, Infant, medicine.disease, Newborn, agammaglobulinemia, business, Intravenous, Meningitis, Cohort study
Abstract

A questionnaire-based retrospective clinical and immunological survey was conducted in 73 males with a definite diagnosis of X-linked agammaglobulinemia based on BTK sequence analysis. Forty-four were sporadic and 29 familial cases. At December 2000, the patients' ages ranged from 2 to 33 years; mean age at diagnosis and mean duration of follow-up were 3.5 and 10 years respectively. After the mid-1980s all but 2 were on intravenous immunoglobulin (IVIG) substitution therapy, with residual IgG >500 mg/dl in 94% of the patients at the time of enrollment. Respiratory infections were the most frequent manifestation both prior to diagnosis and over follow-up. Chronic lung disease (CLD) was present in 24 patients, in 15 already at diagnosis and in 9 more by 2000. The cumulative risk to present at diagnosis with CLD increased from 0.17 to 0.40 and 0.78 when the diagnosis was made at the ages of 5, 10, and 15 years respectively. For the 9 patients who developed CLD during follow-up, the duration of follow-up, rather than age at diagnosis; previous administration of intramuscular immunoglobulin; and residual IgG levels had a significant effect on the development of CLD. Chronic sinusitis was present in 35 patients (48%), in 15 already at diagnosis and in 20 by 2000. Sistemic infections such as sepsis and meningitis/meningoencephalitis decreased over follow-up, probably due to optimal protection provided by high circulating IgG levels reached with IVIG.

Published
2002

14. An interesting question of Pompe disease. A case report.

Author

Accomando S, Montaperto D, Fragapane ML, Amato GM, Corsello G, Cappello F, and Maresi E

Subjects
Female, Glycogen Storage Disease Type II genetics, Humans, Infant, Liver metabolism, Liver pathology, Glycogen Storage Disease Type II metabolism, Glycogen Storage Disease Type II pathology
Abstract

Glycogenosis type II or Pompe disease is an inherited autosomal recessive disorder known in 3 different clinical forms (infantile, juvenile and adult). We report on a case diagnosed as a classic infantile form with the worst outcome of all 3 described, if we had followed and executed a correct and complete diagnostic pathway. A 7 months old female child was admitted for fever and dyspnoea. At chest auscultation weepings and weezings were found; on the cardiac apex a murmur due to mitralic failure was retrieved. The thorax X-ray showed a greatly increased heart shadow with a cardiothoracic index of 0.75. ECG showed high voltages and signs of bilateral ventricular hypertrophy. Cardiac ultrasonography confirmed the presence of a big heart with an enormous swollen left ventricle and a severe mitralic failure. The clinical diagnosis of infantile Pompe disease was confirmed by the almost total absence of cellular acid a-glucosidase activity but we couldn't perform the assay because of the rapid exitus of our patient, which occurred before glycogen storage disease II was suspected. So, we tried to compare our case with others reported in the literature in order to ratify our diagnostic hypothesis. The contribution of genetic counseling practiced on all the couples at risk remains useful every time that a certain diagnosis is made.

Published
2005

15. Coeliac disease and depression: two related entities?

Author

Accomando S, Fragapane ML, Montaperto D, Trizzino A, Amato GM, Calderone F, and Accomando I

Subjects
Adult, Age Factors, Chi-Square Distribution, Child, Female, Humans, Male, Risk Factors, Sex Factors, Surveys and Questionnaires, Celiac Disease complications, Depression complications
Published
2005
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16. Mycoplasma pneumonias distribution, epidemiology and prevalence in a triennial survey.

Author

Accomando S, Trizzino A, Montaperto D, Barcellona R, and Amato GM

Subjects
Adolescent, Child, Child, Preschool, Humans, Incidence, Infant, Prevalence, Pneumonia, Mycoplasma epidemiology
Abstract

Objectives: To evaluate: (1) the incidence of pneumonia monthly distribution; (2) the rate of pneumonitis due to Mycoplasma Pneumoniae; (3) the suitability of choosing an empirical-based antibiotic-therapy; (4) the need of a critical revision of Mycoplasma serological data., Patients and Methods: We studied 188 patients admitted to the Palermo University Pediatrics Department, from september 1998 to august 2001, with admission diagnosis of pneumonia., Results: The highest incidence of pneumonia was in december and march as in both months 28 cases occurred in the whole period 1998-2001 (average of 9.3 cases per each month). The highest rate of pneumonias by Mycoplasma Pneumoniae was in may with a total number of 11/21 cases (52.3%, average of 3.67 cases per month) in the above mentioned three-year period., Conclusions: Incidence of Mycoplasma pneumonitis is more represented in subjects that are at school age. Our study confirms the enormous variability of the prevalence of the infection by Mycoplasma Pneumoniae and how difficult it is to make an accurate diagnosis lacking standardized, rapid, specific and comparative methods.

Published
2004

17. Two strange cases of hypereosinophilia and child's relapsing angio-oedema.

Author

Accomando S, Caserta M, Trizzino A, and Amato GM

Subjects
Angioedema parasitology, Child, Preschool, Cysticercosis complications, Eosinophilia parasitology, Female, Humans, Male, Recurrence, Angioedema complications, Eosinophilia complications
Abstract

Two patients aged two and four years came to our observation with "angio-oedema" and relapsing hypodermitis. Atopic diseases were present in both family histories. The clinical examination of both children revealed a good nutritional status, the presence of angio-oedema with fleeting (48 hours max length) and localized hypodermic infiltrations. Amongst laboratory investigations, the blood cells count and the total count of Immunoglobulins showed hypereosinophilia and increased IgE levels over ten times the normal values. Prick tests for the most common inhalant and nutritive allergens were negative. A strong positivity of ELISA for Taenia Solium metacestodes on both sera samples suggested a diagnosis of human cysticercosis.

Published
2003

18. [Diagnosis in pediatric "allergic" patients].

Author

Amato GM, Amato G, Barcellona R, Carta M, Giuffré M, Piazza L, and Travia A

Subjects
Adolescent, Child, Eosinophils immunology, Female, Humans, Hypersensitivity immunology, Immunoglobulin E immunology, Male, Retrospective Studies, Skin Tests, Hypersensitivity diagnosis
Abstract

Background: A clinician who deals with allergic patients needs the help of in vivo and in vitro allergometric tests in order to decide difficult therapeutic choices., Methods: In the section of Clinical Immunology of the Institute of Paediatrics (Palermo University) two allergologic tests, prick and MAST-CLA, have been studied retrospectively, they were performed on patients observed for allergic disorders over 5 years. The aim of this study was to evaluate the diagnostic capacity of these tests "on the field". The study population is made of 459 patients (age range from 6 months to 16 years) affected with asthma, rhinitis, presumably allergic dermatitis, association of asthma and dermatitis, urticaria, selected on the basis of anamnesis and clinical examination. Eosynophils, basophils, total IgE, specific IgE with DHS-MAST-CLA and prick tests (Bayropharm) for the allergens most frequently responsible of allergic disease in our country, have been evaluated. A double controlled assay of 1040 pairs of allergens with MAST-CLA has been performed., Results: The agreement between prick and MAST appeared to be satisfactory for inhaled allergens. Eosynophils count and total IgE levels showed a significative difference between patients negative versus patients positive for at least one allergen., Conclusions: The pattern of the allergens most frequently positive changes with age and patients positive for pollens showed positivity for vegetal food allergens with a frequency higher than expected.

Published
1997

19. [Rheumatoid-like syndrome as a symptom of agammaglobulinemia].

Author

Amato GM, Barcellona R, Travia A, and Amato G

Subjects
Agammaglobulinemia drug therapy, Agammaglobulinemia genetics, Child, Preschool, Diagnosis, Differential, Genetic Linkage, Humans, Immunoglobulins, Intravenous therapeutic use, Male, Sex Chromosome Aberrations genetics, X Chromosome, Agammaglobulinemia diagnosis, Arthritis, Rheumatoid diagnosis
Abstract

A case of rheumatoid-like arthritis as a symptom of primary agammaglobulinemia X-linked in a 24-month-old child is reported. The treatment protocol is also discussed.

Published
1997

20. [Lipid pneumonia. Favorable outcome after treatment with intravenous immunoglobulins, steroids, cephalosporins].

Author

Amato GM, Novara V, and Amato G

Subjects
Humans, Infant, Male, Adrenal Cortex Hormones therapeutic use, Cephalosporins therapeutic use, Immunoglobulins, Intravenous therapeutic use, Pneumonia, Lipid drug therapy
Abstract

Lipoid pneumonia. Recovery after treatment with intravenous immunoglobulins, steroids, cephalosporins. A case of lipoid pneumonia is described, due to accidental inhalation of cosmetic oil occurred in an infant 11 months old, which caused severe clinical and radiological features. The patient was treated with antibiotics, corticosteroids and intravenous immunoglobulins. Clinical and radiological recovery was achieved within 5 months and persisted at 9 and 20 months follow-up.

Published
1997

21. [Discitis in childhood: integrated neuroradiological imaging in diagnosis and follow-up study of one case].

Author

Giuffrè M, Amato GM, Manfrè L, and Morello A

Subjects
Anti-Infective Agents administration & dosage, Anti-Infective Agents therapeutic use, Cefotaxime administration & dosage, Cefotaxime analogs & derivatives, Cefotaxime therapeutic use, Cephalosporins administration & dosage, Cephalosporins therapeutic use, Child, Ciprofloxacin administration & dosage, Ciprofloxacin therapeutic use, Discitis drug therapy, Discitis pathology, Female, Humans, Lumbosacral Region pathology, Magnetic Resonance Imaging, Teicoplanin administration & dosage, Teicoplanin therapeutic use, Discitis diagnosis
Abstract

Discitis is an inflammatory disease of the intervertebral disc which has usually a benign evolution in childhood. It often recognizes an infectious etiology. Still discussed however is the possibility of a primitive discal involvement (not secondary to a vertebral inflammation) or of a non infectious etiology and the subsequent more correct diagnostic-therapeutic procedures. We report a case of a girl with discitis diagnosed early and treated with antibiotics and orthopedic corset, whose follow-up shows a benign evolution. We underline the importance of modern neuroradiological imaging: in particular, MR plays a major role in the inflammatory diseases of the column, both in diagnosis and in follow-up. MR scans of the involved disc allow frequent controls without radiogenic risks and with a good resolution because of the multiplanarity typical of the method.

Published
1997

23. [Case of cutaneous mastocytosis].

Author

Amato GM, Collica F, and Puma G

Subjects
Biopsy, Female, Humans, Infant, Urticaria Pigmentosa pathology, Urticaria Pigmentosa diagnosis
Published
1976

24. [Schoenlein-Henoch syndrome. Clinical considerations on 275 cases].

Author

Amato GM, Agozzino A, Di Giorgio MP, and Travia A

Subjects
Child, Child, Preschool, Female, Gastrointestinal Diseases etiology, Humans, IgA Vasculitis diagnosis, IgA Vasculitis therapy, Joint Diseases etiology, Kidney Diseases etiology, Male, Pain etiology, Skin Diseases etiology, IgA Vasculitis complications
Published
1984

26. [Schoenlein-Henoch syndrome. Preliminary study of 152 cases].

Author

Agozzino A, Di Giorgio M, Travia A, and Amato GM

Subjects
Adolescent, Child, Child, Preschool, Female, Follow-Up Studies, Humans, IgA Vasculitis therapy, Immunoglobulin A analysis, Infant, Male, IgA Vasculitis diagnosis
Published
1983

31. [Chronic cobalt poisoning. Presentation of a clinical case of cardiomyopathy].

Author

La Grutta A, Amato GM, Fedele S, and Vitaliti S

Subjects
Anemia, Hypochromic drug therapy, Child, Preschool, Goiter chemically induced, Humans, Iatrogenic Disease, Male, Polycythemia chemically induced, Cardiomyopathy, Dilated chemically induced, Cobalt poisoning, Heart Failure chemically induced
Published
1984

32. [A case of Blackfan-Diamond anemia].

Author

Amato GM, Carnesi MT, and Giuffrè L

Subjects
Child, Preschool, Chromosome Aberrations, Chromosome Disorders, Humans, Karyotyping, Male, Syndrome, Anemia, Aplastic, Erythrocytes, Abnormal, Erythropoiesis
Published
1975

33. [The Silver-Russell syndrome. Report of 2 cases].

Author

Liotta A, Romano MR, Travia A, and Amato GM

Subjects
Child, Female, Humans, Syndrome, Abnormalities, Multiple, Craniofacial Dysostosis, Dwarfism congenital, Limb Deformities, Congenital
Published
1980

34. [Streptococcal infections in thalassemic children].

Author

Amato GM, Barcellona R, Macaluso M, Masseria R, Natoli D, and Palmigiano C

Subjects
Adolescent, Child, Child, Preschool, Humans, Infant, Pharyngitis etiology, Rheumatic Fever etiology, Streptococcal Infections complications, Thalassemia complications
Published
1980

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