116 related articles for article (PubMed ID: 14348413)
1. [FREQUENCY OF VARIOUS TYPES OF MICROCYTHEMIA AND ABNORMAL HEMOGLOBINS IN THE PROVINCE OF LECCE].
SILVESTRONI E; BIANCO I; MURATORE F
Prog Med (Napoli); 1965 Apr; 21():211-6. PubMed ID: 14348413
[No Abstract] [Full Text] [Related]
2. [PRESENCE OF MICROCYTHEMIA WITH NORMAL AMOUNT OF HEMOGLOBIN A2 AND ELEVATED AMOUNT OF HEMOGLOBIN F IN A CALABRIAN FAMILY (THIRD VARIETY OF MICROCYTHEMIA)].
SILVESTRONI E; BIANCO I; BRANCATI C
Policlinico Prat; 1964 Oct; 71():1543-5. PubMed ID: 14213722
[No Abstract] [Full Text] [Related]
3. [A CASE OF HEMOGLOBIA DISEASE LEPORE-MICROCYTHEMIA IN A CALABRIAN FAMILY].
BIANCO I; BRANCATI C
Policlinico Prat; 1965 May; 72():661-5. PubMed ID: 14348117
[No Abstract] [Full Text] [Related]
4. INTERACTION OF HEMOGLOBIN LEPORE WITH SICKLE CELL TRAIT AND MICROCYTHEMIA (THALASSEMIA) IN A SOUTHERN ITALIAN FAMILY.
SILVESTRONI E; BIANCO I; BAGLIONI C
Blood; 1965 Apr; 25():457-69. PubMed ID: 14284335
[No Abstract] [Full Text] [Related]
5. [MICROCYTHEMIA AND ABNORMAL HEMOGLOBINS IN CALABRIA].
BRANCATI C; PUCCETTI G
Prog Med (Napoli); 1964 Oct; 20():635-44. PubMed ID: 14260342
[No Abstract] [Full Text] [Related]
6. THE FIRST OBSERVATION OF AN ABNORMAL HAEMOGLOBIN IN A JEWISH FAMILY: HAEMOGLOBIN BEILINSON.
DEVRIES A; JOSHUA H; LEHMANN H; HILL RL; FELLOWS RE
Br J Haematol; 1963 Oct; 9():484-6. PubMed ID: 14076130
[No Abstract] [Full Text] [Related]
7. HEREDITARY PERSISTENCE OF FOETAL HAEMOGLOBIN IN COMBINATION WITH THALASSEMIA IN TWO INDIAN FAMILIES.
PAREKH JG; SHARMA RS; SHAH KM
J Assoc Physicians India; 1963 Dec; 11():975-81. PubMed ID: 14086077
[No Abstract] [Full Text] [Related]
8. [A CASE OF MICRODREPANOCYTIC DISEASE DUE TO S HEMOGLOBIN AND A VARIETY OF MICROCYTHEMIA WITH NORMAL QUOTA OF A2 HEMOGLOBIN AND ELEVATED QUOTA OF F HEMOGLOBIN (THIRD VARIETY OF MICRODREPANOCYTIC DISEASE)].
SILVESTRONI E; BIANCO I
Prog Med (Napoli); 1964 Aug; 20():509-13. PubMed ID: 14235120
[No Abstract] [Full Text] [Related]
9. [FIRST CASE OF THE HB LEPORE DISEASE WITH MICROCYTHEMIA OBSERVED IN ITALY].
SILVESTRONI E; BIANCO I
Policlinico Prat; 1963 Oct; 70():1513-7. PubMed ID: 14094667
[No Abstract] [Full Text] [Related]
10. [CONCERNING A CASE OF TYPICAL REGIONAL PATHOLOGY: THE FIRST CASE IN SARDINIA OF COMBINED HEMOGLOBIN H DISEASE AND THALASSEMIA].
FIASCHI E; CAMPANACCI L; NACCARATO R
Minerva Med; 1964 May; 55():1717-24. PubMed ID: 14175655
[No Abstract] [Full Text] [Related]
11. [DESCRIPTION OF A NEW SLOW HEMOGLOBIN IN A CASERTIAN FAMILY (HB CASERTA)].
VENTRUTO V; DEROSA L; BIANCHI P; RICCHI L; QUATTRIN N
Prog Med (Napoli); 1964 Mar; 20():157-62. PubMed ID: 14216869
[No Abstract] [Full Text] [Related]
12. Prevalence of beta-thalassemia trait and abnormal hemoglobins in the province of Adıyaman, Turkey.
Genc A; Tastemir Korkmaz D; Urhan Kucuk M; Rencuzogullari E; Atakur S; Bayram S; Onderci M; Koc T; Aslan S; Mutalip A; Faruk M; Sevgiler Y; Tuncdemir A
Pediatr Hematol Oncol; 2012 Oct; 29(7):620-3. PubMed ID: 22897698
[TBL] [Abstract][Full Text] [Related]
13. [CONSIDERATIONS ON 4 CASES WITH ABNORMAL HEMOGLOBINS DISCOVERED AT THE "BACH-MAI" TRAINING HOSPITAL OF THE FACULTY OF MEDICINE OF HANOI].
BACHQUOC TUYEN ; DANGVAN AN; PHAMNGOC TRONG ; DANGDUC QUI ; NGUYENDINH LUONG
Med Interna (Bucur); 1964 Oct; 16():1187-93. PubMed ID: 14244197
[No Abstract] [Full Text] [Related]
14. Prevalence of β-thalassemia trait and abnormal hemoglobins in Sanliurfa Province in southeast Turkey.
Incebiyik A; Genc A; Hilali NG; Camuzcuoglu A; Camuzcuoglu H; Kilic A; Vural M
Hemoglobin; 2014; 38(6):402-4. PubMed ID: 25405917
[TBL] [Abstract][Full Text] [Related]
15. [HEMOGLOBIN H IN TURKEY].
GOEKSEL V; BOELUEKOGLU MA; AKPINAR N; ASLAN M; TARTAROGLU N
Blut; 1964 Sep; 10():185-9. PubMed ID: 14282889
[No Abstract] [Full Text] [Related]
16. [Clinical, genetic and biochemical findings on some hemoglobinopathies (Hb H-microcythemia; Hb Cagliari-microcythemia) in the Sardinian population].
Sulis E; Alessio L; Medda A
Minerva Med; 1966 Oct; 57(79):3179-88. PubMed ID: 5926096
[No Abstract] [Full Text] [Related]
17. [Microcythemia with abundant Hb F and normal Hb A2 in three families of Puglie].
Silvestroni E; Bianco I
Policlinico Prat; 1965 Oct; 72(41):1381-8. PubMed ID: 5856487
[No Abstract] [Full Text] [Related]
18. [A case of association of hemoglobin D-beta microcythemia].
Oldrini R; Salmini G; Maioio AT
Haematologica; 1972; 58(9):515-21. PubMed ID: 4206223
[No Abstract] [Full Text] [Related]
19. [AN INVESTIGATION OF ABNORMAL HEMOGLOBINS IN SOUTHERN JAPAN. 1. A CASE OF THALASSEMIA MINOR DISCOVERED ON AMAMI ISLANDS].
OHTA Y
Jinrui Idengaku Zasshi; 1963 Sep; 8():227-38. PubMed ID: 14115915
[No Abstract] [Full Text] [Related]
20. SICKLE CELL THALASSAEMIA: A REPORT OF FOUR CASES IN THREE MEDITERRANEAN FAMILIES LIVING IN AUSTRALIA.
COWLING DC; UNGAR B; BAIRD CW
Med J Aust; 1965 Jul; 2(2):75-9. PubMed ID: 14326767
[No Abstract] [Full Text] [Related]
[Next] [New Search]