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Results of search for 'au:"MOLLICA, F"', page 3 of 7
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Authors
Antener, I
Bosco, P
Cavallaro, N
Di Bella, D
Di Martino, L
Distefano, G
Garozzo, R
Gorgone, G
Grasso, A
Incorpora, G
La Rosa, M
Li Volti, S
MOLLICA, F
Mattina, T
Mazzone, D
Mollica, F
Musumeci, S
Pavone, L
Russo, G
Sorge, G
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Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Female
Genes, Dominant
Humans
Infant
Infant, Newborn
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Pedigree
Pregnancy
Sicily
abnormalities
analysis
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complications
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genetics
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41.
Viral hepatitis B and Wiskott-Aldrich syndrome.
[electronic resource]
by
Musumeci, S
Sciotto, A
Fischer, A
Mollica, F
Producer:
19800324
In:
Helvetica paediatrica acta
vol. 34
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42.
Infantile spasms syndrome in monozygotic twins. A 7-year follow-up.
[electronic resource]
by
Pavone, L
Mollica, F
Incorpora, G
Pampiglione, G
Producer:
19860320
In:
Italian journal of neurological sciences
vol. 6
Online resources:
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43.
A prospective study of 18 infants of chronic HBsAg mothers.
[electronic resource]
by
Mollica, F
Musumeli, S
Rugolo, S
Mattina, T
Producer:
19800119
In:
Archives of disease in childhood
vol. 54
Online resources:
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44.
Hemolytic crises of favism in Sicilian females heterozygous for G-6-PD deficiency.
[electronic resource]
by
Russo, G
Mollica, F
Pavone, L
Schilirò, G
Producer:
19720911
In:
Pediatrics
vol. 49
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45.
[10 families with benign familial hematuria. Considerations on prevalence, genetics and clinical and urine characteristics].
[electronic resource]
by
Li Volti, S
D'Avola, M A
Mollica, F
Producer:
19900206
In:
Minerva pediatrica
vol. 41
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46.
Maternal transmission of HBV infection.
[electronic resource]
by
Mollica, F
Musumeci, S
Mattina, T
Rugolo, S
Producer:
19800425
In:
Pediatrics
vol. 65
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47.
A case of cyclopia. Role of environmental factors.
[electronic resource]
by
Mollica, F
Pavone, L
Nuciforo, G
Sorge, G
Producer:
19791121
In:
Clinical genetics
vol. 16
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48.
Immuno-deficiency in Schwartz-Jampel syndrome.
[electronic resource]
by
Mollica, F
Messina, A
Stivala, F
Pavone, L
Producer:
19790223
In:
Acta paediatrica Scandinavica
vol. 68
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49.
Infantile spasms syndrome in monozygotic twins.
[electronic resource]
by
Pavone, L
Mollica, F
Incorpora, G
Pampiglione, G
Producer:
19810129
In:
Archives of disease in childhood
vol. 55
Online resources:
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50.
Familial centronuclear myopathy.
[electronic resource]
by
Pavone, L
Mollica, F
Grasso, A
Pero, G
Producer:
19810521
In:
Acta neurologica Scandinavica
vol. 62
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51.
IgA in twenty-nail dystrophy.
[electronic resource]
by
Mollica, F
Pavone, L
LiVolti, S
Guarneri, B
Producer:
19831008
In:
The Journal of pediatrics
vol. 103
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52.
Intrathecal methotrexate.
[electronic resource]
by
Mollica, F
Schilirò, G
Pavone, L
Collica, F
Producer:
19711202
In:
Lancet (London, England)
vol. 2
Online resources:
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53.
Congenital lactose intolerance of gastrogen origin associated with cataracts.
[electronic resource]
by
Russo, G
Mollica, F
Mazzone, D
Santonocito, B
Producer:
19740823
In:
Acta paediatrica Scandinavica
vol. 63
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54.
Robins's syndrome in three children of consanguineous parents. A pedigree suggesting autosomal recessive inheritance.
[electronic resource]
by
Russo, G
Mollica, F
Pavone, L
Musumeci, S
Producer:
19740429
In:
Acta geneticae medicae et gemellologiae
vol. 21
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55.
Effectiveness of early prednisone treatment in preventing the development of nephropathy in anaphylactoid purpura.
[electronic resource]
by
Mollica, F
Li Volti, S
Garozzo, R
Russo, G
Producer:
19920402
In:
European journal of pediatrics
vol. 151
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56.
["Normal-trisomy 21" mosaicism].
[electronic resource]
by
Pavone, L
Garozzo, S
Di Gregorio, L
Mollica, F
Producer:
19751120
In:
La Pediatria
vol. 82
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57.
[A case of severe renal tubular acidosis in an infant].
[electronic resource]
by
Mollica, F
Panebianco, M G
Pavone, L
Turlà, B
Producer:
19760706
In:
La Pediatria
vol. 83
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58.
[Preliminary results of the study of the electrical activity of the colon in children].
[electronic resource]
by
Di Martino, L
Mollica, F
Gula, G
Pisano, M
Producer:
19710823
In:
Bollettino della Societa italiana di biologia sperimentale
vol. 46
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59.
Corticosteroid therapy does not prevent nephritis in Henoch-Schönlein purpura.
[electronic resource]
by
Mollica, F
Li Volti, S
Garozzo, R
Russo, G
Producer:
19940504
In:
Pediatric nephrology (Berlin, Germany)
vol. 8
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60.
Severe case of Al Awadi/Raas-Rothschild syndrome or new, possibly autosomal recessive facio-skeleto-genital syndrome.
[electronic resource]
by
Mollica, F
Mazzone, D
Cimino, G
Opitz, J M
Producer:
19950828
In:
American journal of medical genetics
vol. 56
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