-transparent.png){kind=logo}
Two patients had neovascularizations, bleeding and enclosed vessels or pigmented foci on the retina. The analysis of the hemoglobin showed a raised HbA2 fraction, indicating that they could be considered heterozygous gene carriers of beta-thalassemia. An electrophoretic-spectrophotometric method of determining the hematologic changes is described by means of which thalassemia minima can be diagnosed reliably.
Related Publications
W Hammerstein, and
J Scheja, and
H Brüster, and
H Trobisch, and
G Bischof, and
H Kramp
September 1980,
Klinische Monatsblatter fur Augenheilkunde,
W Hammerstein, and
J Scheja, and
H Brüster, and
H Trobisch, and
G Bischof, and
H Kramp
February 1974,
[Rinsho ketsueki] The Japanese journal of clinical hematology,
W Hammerstein, and
J Scheja, and
H Brüster, and
H Trobisch, and
G Bischof, and
H Kramp
November 1977,
Klinika oczna,
W Hammerstein, and
J Scheja, and
H Brüster, and
H Trobisch, and
G Bischof, and
H Kramp
January 1974,
Klinische Monatsblatter fur Augenheilkunde,
W Hammerstein, and
J Scheja, and
H Brüster, and
H Trobisch, and
G Bischof, and
H Kramp
November 1976,
Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie. Albrecht von Graefe's archive for clinical and experimental ophthalmology,
W Hammerstein, and
J Scheja, and
H Brüster, and
H Trobisch, and
G Bischof, and
H Kramp
March 1982,
La Pediatria,
W Hammerstein, and
J Scheja, and
H Brüster, and
H Trobisch, and
G Bischof, and
H Kramp
January 1981,
La Pediatria medica e chirurgica : Medical and surgical pediatrics,
W Hammerstein, and
J Scheja, and
H Brüster, and
H Trobisch, and
G Bischof, and
H Kramp
January 1981,
Bratislavske lekarske listy,
W Hammerstein, and
J Scheja, and
H Brüster, and
H Trobisch, and
G Bischof, and
H Kramp
September 1976,
No shinkei geka. Neurological surgery,
W Hammerstein, and
J Scheja, and
H Brüster, and
H Trobisch, and
G Bischof, and
H Kramp
January 1981,
Klinika oczna,
