A. Rasore-Quartino

发表

Dyskeratosis congenita: unusual presenting features within a kindred.

G. Forni, C. Melevendi, S. Jappelli, 1993, Pediatric hematology and oncology.

[Atypical form of malignant hyperthermia. Observation of a case caused by ketamine].

A. Rasore-Quartino, P. de Bellis, F. Bertamino, 1985, Pathologica.

The adult with Down syndrome : a new challenge for society

J. Rondal, S. Soresi, A. Rasore-Quartino, 2004 .

[Hemophilia and von Willebrand's disease. (Recent acquisitions)].

A. Rasore-Quartino, G. Gastaldi, 1976, Pathologica.

Coexistence of haemophilia A and von Willebrand's disease in the same kindred.

P. Mannucci, A. Campanella, A. Galletti, 2009, Scandinavian journal of haematology.

Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna.

W. Reardon, W. Hul, W. Wuyts, 2000, Human molecular genetics.

[Concordant MZ mongoloid twins].

A. Rasore-Quartino, 1967, Acta geneticae medicae et gemellologiae.

[Spondylo-epiphyseal dysplasia tarda with progressive arthropathy: description of a patient whose mother showed minimal features of the disease].

A. Camera, A. Rasore-Quartino, G. Camera, 1993, Pathologica.

The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)

W. Wuyts, T. Homfray, F. Vanhoenacker, 2000, Journal of medical genetics.

Hereditary deficiency in pseudo-cholineslerase and apnoea from succinylcholine

A. Rasore-Quartino, G. Sansone, 1966 .

Down syndrome and coeliac disease: usefulness of antigliadin and antiendomysium antibodies

G. Gemme, P. Scartezzini, M. Bonamico, 1996, Acta paediatrica.

[Severely hypoplastic bilateral polycystic kidney associated with other malformations in a newborn infant].

A. Rasore-Quartino, 1965, Pathologica.

TWO RED-CELL POPULATIONS IN THE HUMAN FEMALE HETEROZYGOUS FOR G.-6-P.D. DEFICIENCY

G. Veneziano, A. Rasore-Quartino, G. Sansone, 1964 .

Identification and characterization of a new human gene encoding a small protein with high homology to the proline-rich region of the SH3BGR gene.

P. Arrigo, S. Giglio, P. Scartezzini, 1998, Biochemical and biophysical research communications.

Identification and characterization of a new human cDNA from chromosome 21q22.3 encoding a basic nuclear protein

D. Nižetić, F. Sotgia, P. Arrigo, 1998, Human Genetics.

Cloning a new human gene from chromosome 21q22.3 encoding a glutamic acid-rich protein expressed in heart and skeletal muscle

D. Nižetić, S. Colella, R. Taramelli, 1997, Human Genetics.

[DEMONSTRATION ON BLOOD SMEARS OF A DOUBLE ERYTHROCYTE POPULATION IN WOMEN HETEROZYGOUS FOR GLUCOSE-6-P DEHYDROGENASE DEFICIENCY].

G. Veneziano, A. Rasore-Quartino, G. Sansone, 1963, Pathologica.

[Familial ataxia with peroneal muscular atrophy and optic atrophy].

A. Rasore-Quartino, G. Bernabò Brea, R. Rathschüler, 1966, Rivista oto-neuro-oftalmologica.

[The Pierre Robin syndrome. Study of 7 cases].

A. Rasore-Quartino, A. Centa, 1967, Minerva pediatrica.

[Pseudo-Pelger anomaly during acute leukemia in a child].

A. Rasore-Quartino, 1967, Pathologica.

[Giant thymus hyperplasia in childhood].

A. Rasore-Quartino, G. Romagnoli, F. Rebizzo, 1979, Pathologica.

Th ERYTHROCYTE POLYAGGLUTINATION

G. Veneziano, A. Rasore-Quartino, G. Sansone, 1978, The Lancet.