H. Lehmann

发表

Haemoglobin Hammersmith (beta-42 (CDI) Phe replaced by ser).

P. Gaffney, J. Dacie, N. Shinton, 1967, Nature.

Abnormal haemoglobins in Iran. Observation of a new variant--haemoglobin J Iran (alpha-2-beta-2 77 His--Asp).

H. Lehmann, S. Rahbar, D. Beale, 1967, British medical journal.

Hereditary persistence of fetal hemoglobin, beta thalassemia, and the hemoglobin delta-beta locus: further family data and genetic interpretations.

A. Motulsky, H. Lehmann, N. Bethlenfalvay, 1975, American journal of human genetics.

Haemoglobin gene frequencies in the Jamaican population: a study in 100,000 newborns

D. Higgs, H. Lehmann, G. Serjeant, 1986, British journal of haematology.

Two new pathological haemoglobins: Olmsted beta 141 (H19) Leu leads to Arg and Malmö beta 97 (FG4) His leads to Gln.

H. Lehmann, P. Lorkin, 1970, The Biochemical journal.

The myoglobin of primates. VIII. Nycticebus coucang (slow loris).

H. Lehmann, A. E. Romero-Herrera, O. Castillo, 1976, Biochimica et biophysica acta.

Haemoglobin Tak: a β‐Chain Elongation

K. Imai, P. Vinai, H. Lehmann, 1975 .

The primary structure of the myoglobin of Didelphis marsupialis (Virginia opossum).

H. Lehmann, A. E. Romero-Herrera, 1975, Biochimica et biophysica acta.

Haemoglobin titusville: α94 Asp → Asn: A new haemoglobin with a lowered affinity for oxygen

K. Nagai, H. Lehmann, P. Lorkin, 1975 .

The myoglobin of primates. V. Prosimians: Galago crassicaudatus (thick-tailed galago) and Lepilemur mustelinus (sportive lemur).

H. Lehmann, A. R. Romero Herrera, 1973, Biochimica et biophysica acta.

The myoglobin of primates. 4. New World monkeys: Cebidae: (1) Saimiri sciureus (squirrel monkey); (2) Lagothrix lagothricha (Humboldt's woolly monkey). Callitrichidae: Callithrix jacchus (common marmoset).

H. Lehmann, A. Herrera, 1973, Biochimica et biophysica acta.

The myoglobin of primates. I. Hylobates agilis (gibbon).

H. Lehmann, A. R. Romero Herrera, 1971, Biochimica et biophysica acta.

Haemoglobins of Sheep

E. M. Tucker, H. Lehmann, D. Beale, 1966, Nature.

Abnormal Haem Binding and Globin SH Group Blockade in Unstable Haemoglobins

H. S. Jacob, J. Dacie, H. Lehmann, 1968, Nature.

Haemoglobin Sogn (β14 Arginine) A New Haemoglobin Variant

P. Gaffney, H. Lehmann, E. Monn, 2009 .

Evolution of Myoglobin Amino Acid Sequences in Primates and Other Vertebrates

A. Friday, H. Lehmann, A. E. Romero-Herrera, 1976 .

The Second Variant of Human Myoglobin; 138 (H16) Arginine → Glutamine

H. Lehmann, P. Lorkin, F. Boulton, 1971 .

Haemoglobin Dhofar--a new variant from Southern Arabia.

H. Lehmann, P. Lorkin, A. Marengo-Rowe, 1968, Biochimica et biophysica acta.

Haemoglobin J Cape Town—α2 92 Arginine→Glutamine β2

H. Lehmann, D. Beale, W. Isaacs, 1966, Nature.

‘Multiple’ Hæmoglobins in the Horse

H. Lehmann, A. Bangham, 1958, Nature.

Absence of the Sickle Cell Trait in Seventy-two Australian Aboriginals

H. Lehmann, W. Horsfall, 1953, Nature.

The Absence of Haemoglobin C in 104 East Africans living in Dar es Salaam.

H. Lehmann, J. Mackey, 1955 .

Absence of Abnormal Hæmoglobins in some Australian Aboriginals

H. Lehmann, W. Horsfall, 1956, Nature.

A survey for haemoglobin variants, thalassaemia and glucose-6-phosphate dehydrogenase deficiency in northern Ghana.

H. Lehmann, B. Ringelhann, F. Konotey-Ahulu, 1968 .

HAEMOGLOBIN J BALTIMORE INTERACTING WITH BETA‐THALASSAEMIA IN AN AUSTRALIAN FAMILY

H. Kronenberg, H. Lehmann, W. Isaacs, 1967, The Medical journal of Australia.

THE SECOND OBSERVATION OF HAEMOGLOBIN NORFOLK OCCURRING IN AN ITALIAN FAMILY TOGETHER WITH BETA–THALASSAEMIA

H. Kronenberg, H. Lehmann, D. Beale, 1967, The Medical journal of Australia.

The effect of magnesium on blood coagulation in human subjects.

H. Lehmann, R. Huntsman, H. Anstall, 1959, Lancet.

Hyperlipoproteinaemia classification: the optimum routine electrophoretic system and its relevance to treatment.

H. Lehmann, J. Lines, 1972, Lancet.

Haemoglobin North Shore‐Caracas β134 (H12) valine → glutamic acid

H. Lehmann, R. Stathopoulou, T. Arends, 1977 .

Hemoglobin Riyadh-α2β2 (120 [GH3] Lys→Asn): A New Variant Found in Association with α-Thalassemia and Iron Deficiency

H. Lehmann, M. El-Hazmi, 1976 .

Benign Obstetric History in Women with Sickle-cell Anaemia Associated with α-Thalassaemia

H. Lehmann, J. White, A. Lang, 1972, British medical journal.

RAPID ESTIMATION (2 1/2 HOURS) OF GLYCOSYLATED HÆMOGLOBIN FOR ROUTINE PURPOSES

H. Lehmann, P. Kynoch, P.A.M. Kynoch, 1977, The Lancet.

The unstable haemoglobin haemolytic anaemias.

H. Lehmann, R. Carrell, Carrell Rw, 1969, Seminars in hematology.

Selection at molecular level in mammalian myoglobins

R. Diamond, H. Lehmann, O. Castillo, 1978, FEBS letters.

Different types of alpha-thalassaemia and significance of haemoglobin Bart's in neonates.

H. Lehmann, 1970, Lancet.

Beta-Thalassaemia and Some Rare Haemoglobin Variants in the Highlands of Scotland

H. Lehmann, I. A. Cook, 1973, Scottish medical journal.

Hemoglobin winnipeg: Ά275 Asp → Tyr β2

H. Lehmann, F. Vella, P. Galbraith, 1973 .

Hemoglobin Winnipeg: alpha2 75 Asp leads to Tyr beta2.

H. Lehmann, F. Vella, P. Galbraith, 1973, Clinical biochemistry.

The myoglobin of primates. II. Pan Troglodytes (chimpanzee).

H. Lehmann, A. R. Romero Herrera, 1972, Biochimica et biophysica acta.

Paradoxical Effect of Magnesium Ions on Blood Coagulation

H. Lehmann, R. Huntsman, B. Hurn, 1960, Nature.

Hemoglobin Manitoba: α102(G9) serine replaced by arginine

H. Lehmann, J. Kinderlerer, J. Crookston, 1970 .

HEMOGLOBIN G SASKATOON: β22Glu → Ala

H. Lehmann, F. Vella, W. Isaacs, 1967 .

Haemoglobin J Tongariki (alpha-115 alanine--aspartic acid): the first new haemoglobin variant found in a Pacific (Melanesian) population.

D. Irvine, R. Kirk, R. Carrell, 1967, Journal of medical genetics.

N‐terminal chain elongation as evidence for duplication of myoglobin in three South American Monkeys

H. Lehmann, A. Herrera, 1973, FEBS letters.

The myoglobin of primates. 3. Cercopithecidae (Old World monkeys): Papio anubis (olive baboon) and Macaca fascicularis (=irus, crab-eating monkey).

H. Lehmann, A. Herrera, 1972, Biochimica et biophysica acta.

Haemoglobin A′2 : α2δ216 Glycine→Arginine

A. Stretton, H. Lehmann, D. Beale, 1966, Nature.

Abnormal haemoglobins in zambia. A new haemoglobin zambia α60 (E9) lysine→Asparagine

D. Charlesworth, H. Lehmann, G. Barclay, 1969 .

Haemoglobin D Punjab (D Los Angeles)

H. Lehmann, F. Vella, 1974, Journal of medical genetics.

OBSERVATIONS ON THE EFFECT OF MAGNESIUM ON BLOOD COAGULATION

H. Lehmann, R. Huntsman, B. Hurn, 1960, Journal of clinical pathology.

Blood Groups and Enzymes of Human Red Cells after Two Years' Storage in Liquid Nitrogen

H. Lehmann, R. Huntsman, B. Hurn, 1963, British medical journal.

Homozygosity for the d -Chain Variant Haemoglobin A 2 ? (Hbb 2 )(? 16 Gly?Arg)

T. Jenkins, H. Lehmann, G. Nurse, 1985 .

Malignant hyperthermia in pigs: A search for abnormalities in Ca2+ binding proteins

H. Lehmann, P. Lorkin, 1983, FEBS letters.

Gamma Chain Variants in Jamaican Newborns

H. Lehmann, P. Darbre, G. Serjeant, 1976 .

The ξ‐chain, an α‐like chain of human embryonic haemoglobin

H. Lehmann, H. Kamuzora, R. Jones, 1974 .

New Unstable Haemoglobin Borås: β88 (F4) Leucine→Arginine

H. Lehmann, P. Lorkin, Å. Hollender, 1969, Nature.

Hereditary non-spherocytic haemolytic anaemia with post-splenectomy inclusion bodies and pigmenturia caused by an unstable haemoglobin Santa Ana-beta-88 (F4) leucine--proline.

H. Lehmann, P. Lorkin, R. Opfell, 1968, Journal of medical genetics.

I Haemoglobin J Tongariki ( a II Alanine-- Aspartic Acid ) : the first new haemoglobin variant found in a Pacific ( Melanesian ) population

D. Irvine, R. Kirk, D. Gajdusek, 2022 .

Hæmoglobin P in a Family in the Belgian Congo

H. Lehmann, J. Vandepitte, P. Dherte, 1959, Nature.

Three Varieties of Human Hæmoglobin D

S. Benzer, V. Ingram, H. Lehmann, 1958, Nature.

The amino acid sequence of human myoglobin and its minor fractions

H. Lehmann, A. E. Romero-Herrera, A. Romero‐Herrera, 1974, Proceedings of the Royal Society of London. Series B. Biological Sciences.

β-THALASSÆMIA, GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY, AND HÆMOGLOBIN D-PUNJAB IN PATHANS

H. Lehmann, M. A. Stern, P. Kynoch, 1968 .

α‐Thalassaemia as a Cause of Hydrops Foetalis

H. Lehmann, L. L. Eng, L. Gie, 1962 .

alpha-Thalasaemia as a cause of hydrops foetalis.

H. Lehmann, L. Lie-injo, J. Ager, 1962, British journal of haematology.

The Clinical and Haematological Findings in Children Inheriting Two Types of Thalassaemia: High‐A2 Type β‐Thalassaemia, and High‐F Type or δβ‐Thalassaemia

H. Lehmann, C. Kattamis, A. Metaxotou-Mavromati, 1973 .

Abnormal Human Hæmoglobins: Hæmoglobin ‘Bart's’: a Fœtal Hæmoglobin without α-Chains

H. Lehmann, J. Hunt, J. Hunt, 1959, Nature.

Haemoglobin "Bart's': a foetal haemoglobin without alpha-chains.

H. Lehmann, J. Hunt, 1959, Nature.

Urinary amino acids and calcium in relation to renal stones and renal damage.

H. Lehmann, D. B. Roos, R. Huntsman, 1962, Clinical science.

A New Haemoglobin, D Ibadan (β-87 Threonine → Lysine), Producing No Sickle-Cell Haemoglobin D Disease with Haemoglobin S

D. Irvine, H. Lehmann, D. Beale, 1965, Nature.

Urinary excretion of acid muco-polysaccharide in sibs with Morquio's syndrome and Reilly's granules in leucocytes.

H. Lehmann, N. Matsaniotis, C. Kattamis, 1967, Archives of disease in childhood.

Haemoglobin F Hull (gamma-121 glutamic acid--lysine), homologous with haemoglobins O Arab and O Indonesia.

H. Lehmann, D. Beale, P. Lorkin, 1967, British medical journal.

New unstable haemoglobin (Hb Moscva, β24 (B4) Gly→Asp) found in the USSR

H. Lehmann, N. Didkowsky, P. Lorkin, 1974, Nature.

Myoglobin in Primary Muscular Disease: I. Duchenne Muscular Dystrophy: and: II. Muscular Dystrophy of Distal Type

B. Tomlinson, H. Lehmann, J. Walton, 1973, Journal of medical genetics.

Myoglobin in Primary Muscular Disease

H. Lehmann, A. E. Romero-Herrera, E. B, 2022 .

Dystrophy of Distal Type Dystrophy : and : II . Muscular Disease : I . Duchenne Muscular Myoglobin in Primary Muscular

B. Tomlinson, H. Lehmann, A. E. Romero-Herrera, 2022 .

The primary structure of the myoglobin of the insectivore Erinaceus europaeus (common European hedgehog).

H. Lehmann, A. E. Romero-Herrera, W. Fakes, 1975, Biochimica et biophysica acta.

Molecular Pathology of Human Haemoglobin: Stereochemical Interpretation of Abnormal Oxygen Affinities

M. Perutz, H. Morimoto, H. Lehmann, 1971, Nature.

Primary structure of human myoglobin.

H. Lehmann, A. Herrera, 1971, Nature: New biology.

A human myoglobin variant 133 (H-10)lysine--asparagine.

H. Lehmann, P. Lorkin, A. R. Romero Herrera, 1971, Biochimica et biophysica acta.

The third variant of human myoglobin showing an unusual amino acid substitution: 138(H16)arginine--tryptophan.

H. Lehmann, P. Lorkin, A. R. Romero Herrera, 1971, Biochimica et biophysica acta.

Abnormal Human Myoglobin: 53 (D4) Glutamic Acid→Lysine

H. Lehmann, P. Lorkin, F. Boulton, 1969, Nature.

Haemoglobin GCopenhagen and haemoglobin JCambridge. Two new β-chain variants of haemoglobin A

D. Irvine, H. Lehmann, D. Beale, 1967 .

H. Lehmann, M. Farmer, D. N. Raine, 1964, Lancet.

High Resolution Nuclear Magnetic Resonance Studies of Haemoglobin J Capetown

S. Ogawa, H. Lehmann, P. Kynoch, 1970, Nature.

Molecular Pathology of Human Haemoglobin

M. Perutz, H. Lehmann, M. F. PERUTZ, 1968, Nature.

Incidence of Pseudocholinesterase Variants in Australian Aborigines

H. Lehmann, W. Horsfall, D. Davies, 1963, Nature.

A New Hb Variant: Hb F Sardinia γ75 (e 19) Isoieucine→Threonine Found in a Family with Hb G Philadelphia, β-Chain Deficiency and a Lepore-Like Haemoglobin Indistinguishable from Hb A2

D. Charlesworth, H. Lehmann, V. Grifoni, 1975 .

Twelve families with Hb 0 Arab in the Burgas district of Bulgaria observations on sixteen examples of Hb 0 β° thalassaemia

H. Lehmann, R. Casey, K. Kantchev, 2004, Humangenetik.

Haemoglobin O Arab in Sudanese

H. Lehmann, F. Vella, D. Beale, 1966, Nature.

Chemical Heterogeneity of Hæmoglobin O

C. Baglioni, H. Lehmann, 1962, Nature.

Abnormal haemoglobins in Iran. Observation of a new variant haemoglobin J. Iran (α2 β2 77 His -> Asp).

H. Lehmann, S. Rahbar, D. Beale, 1967 .

Hemoglobin I in an American Negro family: structural and hematologic studies.

H. Lehmann, D. Beale, R. Schneider, 1966, The Journal of laboratory and clinical medicine.

Abnormal Haemoglobins and the Genetic Code

H. Lehmann, D. Beale, 1965, Nature.

Synthesis of Hb Lepore ( 2 2 ): influence of and nucleotide sequence on synthesis of chain.

H. Lehmann, J. White, A. Lang, 1972, Nature: New biology.

TREATMENT OF SICKLE‐CELL DISEASE

H. Lehmann, R. Huntsman, 1974, British journal of haematology.

A Ghanaian adult, homozygous for hereditary persistence of foetal haemoglobin and heterozygous for elliptocytosis.

H. Lehmann, B. Ringelhann, F. Konotey-Ahulu, 1970, Acta haematologica.

Globin synthesis in subjects doubly heterozygous for hemoglobin G-Philadelphia and hemoglobin S or C.

H. Lehmann, P. McCurdy, A. Sherman, 1975, The Journal of laboratory and clinical medicine.

Differences between α- and β-Chain Mutants of Human Haemoglobin and between α- and β-Thalassaemia. Possible Duplication of the α-Chain Gene*

H. Lehmann, R. Carrell, 1968 .

Variations in the structure of human haemoglobin. With particular reference to the unstable haemoglobins.

H. Lehmann, R. Carrell, 1969, British medical bulletin.

Haemoglobin Hammersmith (β 42 (CD1) Phe→Ser)

J. Dacie, N. Shinton, H. Lehmann, 1967, Nature.

Homozygous haemoglobin D Punjab.

H. Lehmann, P. Lorkin, A. Lang, 1975, Journal of medical genetics.

d-fl Locus: Further Family Data and Genetic Interpretations

H. Lehmann, N. Bethlenfalvay, B. Ringelhann, 2006 .

INTERACTION OF BETA-THALASSAEMIA AND HEREDITARY PERSISTENCE OF FOETAL HAEMOGLOBIN.

H. Lehmann, G. Bird, O. Malhotra, 1964, Journal of medical genetics.

Further Investigations of the γ-Chain in a Ghanaian Adult, Homozygous for Hereditary Persistence of Fetal Haemoglobin

H. Lehmann, B. Ringelhann, F. Konotey-Ahulu, 1975 .

Is haemoglobin Gα Philadelphia linked to α-thalassaemia?

H. Lehmann, A. Lang, R. Stathopoulou, 1976, Human Genetics.

Hb F Kingston (Gγ55 [D6] Met→Arg)

H. Lehmann, Beryl E. Serjeant, G.R. Serjeant, 1982 .

A new cause of haemolytic anaemia in the newborn. A description of an unstable fetal haemoglobin: F Poole, alpha2-G-gamma2 130 trptophan yeilds glycine.

H. Lehmann, M. Simpkiss, H. Kamuzora, 1975, Journal of clinical pathology.

Haemoglobin F Malaysia: α2γ2 1 (NA1) Glycine→Cysteine; 136 Glycine

H. Lehmann, L. I. Eng, H. Kamuzora, 1974 .

Haemoglobin G-Szuhu, beta80 Asn-Lys, in the homozygous state in a patient with abetalipoproteinaemia.

H. Lehmann, L. Clejan, P. Lorkin, 1975, Human heredity.

HÆmoglobin GAccra

H. Lehmann, D. Beale, F. S. Boi-Doku, 1964, Nature.

Haemoglobin O Arab in Egypt and Aden: possible errors resulting from the use of haemoglobin variants as genetic markers in population surveys.

P. Gaffney, H. Lehmann, R. Huntsman, 1967, Zeitschrift fur Morphologie und Anthropologie.

Chemical heterogeneity of haemoglobin O.

C. Baglioni, H. Lehmann, 1962, Nature.

Two Haemoglobins Q, α74 (EF3) and α75 (EF4) Aspartic Acid→Histidine

D. Charlesworth, H. Lehmann, S. Rahbar, 1970 .

A NEW HEMOGLOBIN VARIANT RESEMBLING HEMOGLOBIN E: HEMOGLOBIN E SASKATOON-β22Glu→Lys

R. Carrell, H. Lehmann, F. Vella, 1967 .

A New Hæmoglobin—Ja Oxford Found During a Survey of an English Population

D. Brown, H. Lehmann, D. Beale, 1964, Nature.

Hb K Woolwich the cause of a thalassaemia

H. Lehmann, A. Lang, P. A. KING-LEWIS, 1974, Nature.

Compensation of chain synthesis by the single chain gene in Hb Lepore trait.

H. Lehmann, J. White, A. Lang, 1972, Nature: New biology.

Hemoglobin S-G (S-D) syndrome.

D. E. Uddin, H. Lehmann, P. Lorkin, 1974, The American journal of medicine.

Haemoglobin Osu-Christiansborg: a new beta-chain variant of haemoglobin A ( beta52 (D3) aspartic acid leads to asparagine) in combination with haemoglobin S.

H. Lehmann, J. Kinderlerer, B. Ringelhann, 1971, Journal of medical genetics.

Haemoglobin K Woolwich (α2β2132 Lysine → Glutamine) in Ghana

H. Lehmann, B. Ringelhann, F. Konotey-Ahulu, 1971 .

Haemoglobin Korle-Bu (beta 73 aspartic acid replaced by asparagine) showing one of the two amino acid substitutions of haemoglobin C Harlem.

H. Lehmann, B. Ringelhann, F. Konotey-Ahulu, 1968, Journal of medical genetics.

Sickle Cell Haemoglobin D Punjab Disease: S from Ghana and D from England

R. Lewis, H. Lehmann, B. Ringelhann, 1967 .

Uncommon Differential Diagnosis to Homozygous Sickle Cell Disease

M. Stevens, H. Lehmann, G. Serjeant, 2016 .

Sickle cell-Hb Lepore Boston syndrome. Uncommon differential diagnosis to homozygous sickle cell disease.

M. Stevens, H. Lehmann, G. Serjeant, 1982, American journal of diseases of children.

The River Niger as a Barrier in the Spread Eastwards of Hæmoglobin C: a Survey of Hæmoglobins in the Ibo

H. Lehmann, C. Nwokolo, 1959, Nature.

Hemoglobin J Cape Town-alpha-2 92 arginine replaced by glutamine beta-2.

H. Lehmann, D. Beale, W. Isaacs, 1966, Nature.

A New Haemoglobin Variant Haemoglobin J Birmingham a 120 (H3) Ala → Glu

J. Mann, H. Lehmann, K. Griffiths, 1974 .

The γ chain of the lamb

H. Lehmann, P. Darbre, 1976 .

Hemoglobin Setif (α94 (G1) ASP → TYR) in Iran a Report of 9 Cases

H. Lehmann, P. Darbre, G. Nozari, 1977 .

Sickling Phenomenon in Deer

K. Betke, H. Lehmann, E. Undritz, 1960, Nature.

Synthesis of haemoglobin Lepore.

H. Lehmann, J. White, J. Reeve, 1972, Nature: New biology.

DUPLICATION OF ALPHA-THALASSÆMIA GENE IN THREE GREEK FAMILIES WITH HÆMOGLOBIN H DISEASE

H. Lehmann, C. Kattamis, 1970 .

Duplication of alpha-thalassaemia gene in three Greek families with haemoglobin H disease.

H. Lehmann, C. Kattamis, 1970, Lancet.

A Haemoglobinopathy Involving Haemoglobin H and a New (Q) Haemoglobin

H. Lehmann, F. Vella, J. Ager, 1958, British medical journal.

Haemoglobin Tak: a variant with additional residues at the end of the beta-chains.

J. Kilmartin, H. Lehmann, J. Kinderlerer, 1971, Lancet.

Hemoglobin Leiden [β6 or 7 (A3 or A4) GLU → 0] in a Yugoslavian Woman Arisen by a New Mutation

H. Lehmann, R. Casey, G. Efremov, 1983 .

Haemoglobin K Woolwich: a study of the family of a homozygote.

H. Lehmann, R. Casey, R. Cabannes, 1980, Journal of medical genetics.

Human skeletal muscle proteins

H. Lehmann, A. E. Romero-Herrera, O. Castillo, 1976, Journal of Molecular Evolution.

Haemoglobin Sydney: β67 (EII) Valine→ Alanine : an Emerging Pattern of Unstable Haemoglobins

H. Lehmann, R. Carrell, P. Lorkin, 1967, Nature.

Haemoglobin Genova: β28 (B10) Leucine→Proline

H. Lehmann, R. Carrell, G. Sansone, 1967, Nature.

Haemoglobin Köln (β–98 Valine → Methionine): An Unstable Protein Causing Inclusion-Body Anaemia

H. Lehmann, R. Carrell, H. Hutchison, 1966, Nature.

A New Haemoglobin, J Toronto (α5 Alanine → Aspartic Acid)

D. Irvine, H. Lehmann, D. Beale, 1965, Nature.

Three Haemoglobins K: Woolwich, an Abnormal, Cameroon and Ibadan, Two Unusual Variants of Human Haemoglobin A

D. Irvine, H. Lehmann, D. Beale, 1965, Nature.

A New Haemoglobin in a Thai Family. A Case of Haemoglobin Siriraj-β Thalassaemia

H. Lehmann, D. Beale, S. Tuchinda, 1965 .

The primary structure of the myoglobin of rabbit (Oryctolagus cuniculus)

H. Lehmann, A. E. Romero-Herrera, O. Castillo, 1976, Biochimica et biophysica acta.

Investigation of malignant hyperthermia: analysis of skeletal muscle proteins from normal and halothane sensitive pigs by two dimensional gel electrophoresis.

H. Lehmann, P. Lorkin, 1983, Journal of medical genetics.

On the evolution of myoglobin.

A. Friday, H. Lehmann, A. E. Romero-Herrera, 1978, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

The myoglobin of the Cape fox (Vulpes chama).

H. Lehmann, O. Castillo, L. T. Jones, 1977, Biochimica et biophysica acta.

Comparison of the myoglobin of the bat-eared fox (Otocyon megalotis) with that of the domestic dog (Canis familiaris).

H. Lehmann, P. Darbre, 1976, Biochimica et biophysica acta.

The myoglobin of the Cape hunting dog (Lycaon pictus).

H. Lehmann, P. Darbre, A. E. Romero-Herrera, 1976, Biochimica et biophysica acta.

Haemoglobin Stanleyville II (alpha asparagine replaced by lysine).

H. Lehmann, D. Beale, G. Van Ros, 1968, British medical journal.

Sickle-Cell Anæmia and Sickle-Cell Trait as Homo- and Heterozygous Gene-Combinations

H. Lehmann, 1951, Nature.

Köln Haemoglobinopathy: FURTHER DATA AND A COMPARISON WITH OTHER HEREDITARY HEINZ BODY ANAEMIAS

H. Lehmann, R. Carrell, A. Grimes, 1967, British journal of haematology.

Haemoglobin P-Nilotic containing a - chain.

H. Lehmann, P. Lorkin, F. Badr, 1973, Nature: New biology.

Sedimentation Characteristics of the γ-Chain Hæmoglobin (Hæmoglobin ‘Bart's’)

H. Lehmann, R. A. Kekwick, 1960, Nature.

Mild “Unstable Haemoglobin Haemolytic Anaemia” caused by Haemoglobin Shepherds Bush (B74 (E18) Gly→Asp)

H. Lehmann, J. White, P. Lorkin, 1970, Nature.

Hemoglobin Etobicoke: α84(F5) serine replaced by arginine.

H. Lehmann, D. Beale, J. Crookston, 1969 .

Haemoglobin Torino – α43 (CDI) Phenylalanine→Valine

H. Lehmann, E. Gallo, A. Beretta, 1968, Nature.

Hereditary Heinz-body Anaemia, Thrombocyttopenia, and Haemoglobinopathy (Hb Köln) in a Glasgow Family

A. S. Douglas, H. Lehmann, D. Beale, 1964, British medical journal.

The First Observation of an Abnormal Haemoglobin in a Jewish Family: Haemoglobin Beilinson

R. Hill, H. Lehmann, R. Fellows, 1963, British journal of haematology.

Hæmoglobin E in Malaya

H. Lehmann, R. Singh, 1956, Nature.

Haemoglobin Ottawa: a215 (Al3) Gly ? Arg 2

H. Lehmann, F. Vella, R. Casey, 1974 .

Molecular Evolution of Myoglobin and the Fossil Record: a Phylogenetic Synthesis

A. Friday, H. Lehmann, A. E. Romero-Herrera, 1973, Nature.

Hb Heathrow: beta G5 103 phenylalanine-leucine: a new high affinity haemoglobin.

H. Lehmann, J. White, P. Lorkin, 1973, British journal of haematology.

An Unstable Haemoglobin with Reduced Oxygen Affinity: Haemoglobin Peterborough, (βiii (G13) Valine → Phenylalanine, its Interaction with Normal Haemoglobin and with Haemoglobin Lepore

H. Morimoto, H. Lehmann, B. Wiltshire, 1972 .

Haemoglobin Buccureşti 42(CD1) Phe-Leu, a cause of unstable haemoglobin haemolytic anaemia.

H. Lehmann, V. Bratu, P. Lorkin, 1971, Biochimica et biophysica acta.

Haemolytic Anaemia due to Haemoglobin Torino

H. Lehmann, U. Mazza, E. Gallo, 1970, British journal of haematology.

THALASSEMIA RESEARCH AND ABNORMAL HEMOGLOBINS

H. Lehmann, R. Huntsman, 1969, Annals of the New York Academy of Sciences.

Haemoglobin hasharon

H. Lehmann, F. Vella, 2004, Humangenetik.

Haemoglobin Nottingham, Beta FG 5 (98) Valgly: A New Unstable Haemoglobin Producing Severe Haemolysis

J. Dacie, H. Lehmann, E. Gordon-Smith, 1973, Proceedings of the Royal Society of Medicine.

Unstable haemoglobin Köln disease in members of a Malay family.

H. Lehmann, C. Lopez, B. Wiltshire, 1972, Journal of medical genetics.

HAEMOGLOBIN KÖLN IN A JEWISH FAMILY

H. Lehmann, J. Hällén, Deborah Charlesworth, 1972, Acta medica Scandinavica.

The genetical interpretation of haemoglobin H disease.

H. Lehmann, C. Kattamis, 1970, Human heredity.

Haemoglobin “Norfolk”: A New Haemoglobin Found in an English Family

H. Lehmann, F. Vella, J. Ager, 1958, British medical journal.

An Abnormal Hæmoglobin in a Chinese: Hæmoglobin G

H. Lehmann, F. Vella, J. Ager, 1958, Nature.

Molecular pathology of human haemoglobin.

M. Perutz, H. Lehmann, 1968, Nature.

Unstable haemoglobin disease caused by Hb Santa Ana- 88 (F4) Leu leads to Pro.

D. Charlesworth, H. Lehmann, P. Lorkin, 1970, Haematologia.

Haemoglobin J Sardegna: α50 (CD 8) Histidine → Aspartic Acid

W. Tangheroni, H. Lehmann, E. Gallo, 1968, Nature.

New Human Haemoglobin Variant from Southern Arabia: G-Audhali (α23(B4) Glutamic Acid→Valine) and the Variability of B4 in Human Haemoglobin

H. Lehmann, D. Beale, A. Marengo-Rowe, 1968, Nature.

Hemoglobin Duarte: (α2β262(E6)Ala→Pro): A New Unstable Hemoglobin With Increased Oxygen Affinity

E. Beutler, H. Lehmann, A. Lang, 1974 .

Haemoglobin Madrid beta 115 (G17) alanine--proline: an unstable variant associated with haemolytic anaemia.

H. Lehmann, J. White, R. Casey, 1974, Acta haematologica.

Haemoglobin Torino--alpha-43 (CD1) phenylalanine replaced by valine.

H. Lehmann, E. Gallo, A. Beretta, 1968, Nature.

Hb altdorf α2β2 135 (H13) Ala → Pro: A new electrophoretically silent unstable haemoglobin variant from switzerland

H. Lehmann, K. Winterhalter, P. Lorkin, 1976 .

The amino acid substitution in Hb olmsted: β141 (H19) leucine → arginine

H. Lehmann, V. Fairbanks, P. Lorkin, 1975 .

An abnormal haemoglobin in a Chinese: haemoglobin G.

H. Lehmann, F. Vella, J. Ager, 1958, Nature.

Zinc acetate as a precipitant of unstable haemoglobins.

H. Lehmann, R. Carrell, 1981, Journal of clinical pathology.

Interaction between Iron Deficiency and α-Thalassaemia: the in vitro Effect of Haemin on α-Chain Synthesis

H. Lehmann, M. El-Hazmi, 1978 .

A new abnormal hemoglobin O Padova, alpha 30 (B11) Glu -- Lys, and a dyserythropoietic anemia with erythroblastic multinuclearity coexisting in the same patient.

H. Lehmann, G. De Sandre, E. D. Di Iorio, 1974, Blood.

Haemoglobin D Ouled Rabah ( p 19 [ B 1 ] Asn-- . Lys ) in a Tuareg tribe of the Southern Sahara

H. Lehmann, A. Mauran-Sendrail, P. Lefèvre-Witier, 2022 .

Observations on haemoglobin P (Congo type).

D. Charlesworth, H. Lehmann, 1970, The Biochemical journal.

Haemoglobin M Saskatoon with slight constant haemolysis, markedly increased by sulphonamides.

H. Lehmann, J. Strömme, P. Lorkin, 2009, Scandinavian journal of haematology.

HÆMOGLOBIN SOUTHAMPTON, β106 (G8) Leu →Pro: AN UNSTABLE VARIANT PRODUCING SEVERE HÆMOLYSIS

H. Lehmann, B. Wiltshire, R. Hyde, 1972 .

Haemoglobin M Hyde Park: a hereditary methaemoglobinaemia in a Caucasian child.

H. Lehmann, R. Carrell, D. Becroft, 1968, The New Zealand medical journal.

New Variant of Human Fœtal Hæmoglobin

H. Lehmann, F. Vella, J. Ager, 1959, Nature.

HÆMOGLOBIN TAK: A VARIANT WITH ADDITIONAL RESIDUES AT THE END OF THE β-CHAINS

J. Kilmartin, H. Lehmann, J. Kinderlerer, 1971 .

Hæmogram, Serum Protein and Plasma Volume of Healthy, Well nourished East Africans in Uganda

H. Lehmann, 1949, Nature.

Public Health and Genetic Constitution of the San (“Bushmen”): Carbohydrate Metabolism and Acetylator Status of the! Kung of Tsumkwe in the North-western Kalahari*

T. Jenkins, H. Lehmann, G. Nurse, 1974, British medical journal.

Haemoglobin coventry (β 141 deleted) in iran

H. Lehmann, S. Rahbar, G. Nozari, 1978 .

Hb Helsinki: a Variant with a High Oxygen Affinity and a Substitution at a 2,3-DPG Binding Site (β82 [EF6] Lys→Met)

K. Nagai, H. Lehmann, P. Pikkarainen, 1976 .

Hb Helsinki: a variant with a high oxygen affinity and a substitution at a 2,3-DPG binding site (beta82[EF6] Lys replaced by Met).

K. Nagai, H. Lehmann, P. Pikkarainen, 1976, Acta haematologica.

Haemoglobin Rahere (beta Lys-Thr): A new high affinity haemoglobin associated with decreased 2, 3-diphosphoglycerate binding and relative polycythaemia.

P. Wrigley, H. Lehmann, A. Stephens, 1975, British medical journal.

An unstable haemoglobin with reduced oxygen affinity: haemoglobin Peterborough, 3 (GI3) Valine lead to Phenylalanine, its interaction with normal haemoglobin and with haemoglobin Lepore.

H. Morimoto, H. Lehmann, B. Wiltshire, 1972, British journal of haematology.

Familial Polycythaemia Caused by a New Haemoglobin Variant: Hb Heathrow, β 103 (G5) Phenylalanine Leucine

H. Lehmann, J. White, I. Gillies, 1973 .

Blood Groups and Enzymes of Human Red Cells After a Year's Storage in Liquid Nitrogen

H. Lehmann, R. Huntsman, B. Hurn, 1962, British medical journal.

Haemoglobin Stanleyville II (α78 Asparagine→Lysine)

H. Lehmann, D. Beale, G. Van Ros, 1968 .

Haemoglobin Titusville: alpha94 Asp replaced by Asn. A new haemoglobin with a lowered affinity for oxygen.

K. Nagai, H. Lehmann, P. Lorkin, 1975, Biochimica et biophysica acta.

The myoglobin of rodents:Lagostomus maximus (viscacha) andSpalax ehrenbergi (mole rat)

E. Nevo, J. O'connell, H. Lehmann, 1984 .

The myoglobin of primates. VII. Perodicticus potto edwarsi (potto).

H. Lehmann, A. E. Romero-Herrera, A. Romero‐Herrera, 1975, Biochimica et biophysica acta.

NOMENCLATURE OF THE α-THALASSAEMIAS

H. Lehmann, R. Carrell, 1984, The Lancet.

Human embryonic haemoglobins including a comparison by homology of the human ζ and α chains

H. Lehmann, H. Kamuzora, 1975, Nature.

Structure and function of a new hemoglobin variant, Hb meilahti (alpha 2 beta 2 36(C2)Pro----Thr), characterized by mass spectrometry.

K. Imai, T. Matsuo, H. Matsuda, 1987, Acta haematologica.

The first observation of Hb D Punjab beta zero thalassaemia in an English family with 22 cases of unsuspected beta zero thalassaemia minor among its members.

H. Lehmann, S. Worthington, 1985, Journal of medical genetics.

Long-Term Preservation of Blood

H. Lehmann, 1964 .

COMPARATIVE STRUCTURE OF MYOGLOBIN: PRIMATES AND TREE‐SHREW

A. Friday, H. Lehmann, K. Joysey, 1974, Annals of the New York Academy of Sciences.

New variant of human foetal haemoglobin.

H. Lehmann, F. Vella, J. Ager, 1959, Nature.

Haemoglobin D Ouled Rabah (beta 19[Bl] asn leads to lys) in a Tuareg tribe of the Southern Sahara.

H. Lehmann, R. Casey, A. Mauran-Sendrail, 1977, Journal of medical genetics.

XI. The hereditary blood factors of the Kurds of Iran.

H. Lehmann, F. Ala, A. Mourant, 1973, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

The oxygen affinity of haemoglobin tak, a variant with an elongated β chain

K. Imai, H. Lehmann, 1975 .

The oxygen affinity of haemoglobin Tak, a variant with an elongated beta chain.

K. Imai, H. Lehmann, 1975, Biochimica et biophysica acta.

Blood Groups of Human Red Cells after Two Years' Storage in Liquid Nitrogen

H. Lehmann, R. Huntsman, B. Hurn, 1964, Transfusion.

Absence of the Diego Blood Group and Abnormal Hæmoglobins in 92 Maoris

H. Lehmann, J. Staveley, A. North, 1958, Nature.

Erythraemia due to Haemoglobin San Diego

I. Chanarin, H. Lehmann, D. Samson, 1975, British journal of haematology.

Differences between alpha- and beta-chain mutants of human haemoglobin and between alpha- and beta-thalassaemia. Possible duplication of the alpha-chain gene.

H. Lehmann, R. Carrell, 1968, British medical journal.

Haemoglobin Stanleyville II (alpha75 [EF 7] Asn yeilds Lys) found in France.

H. Lehmann, P. Darbre, M. North, 1975, Acta haematologica.

Haemoglobin Stanleyville II (α 78 [EF 7] Asn → Lys) Found in France

H. Lehmann, P. Darbre, North Ml, 1975 .

Sickle-cell anaemia.

H. Lehmann, R. Huntsman, 1969, Nursing Times.

Haemoglobin J Paris in the south of Portugal (Algarve).

H. Lehmann, P. Lorkin, C. Trincao, 1968, Acta haematologica.

Hb shaare zedek (α56 E5 Lys → Glu)

H. Lehmann, L. Robb, A. Abramov, 1980 .

Hb Shaare Zedek (alpha 56 E5 Lys leads to Glu).

H. Lehmann, L. Robb, A. Abramov, 1980, FEBS letters.

Haemoglobin Koelliker: A New Acquired Haemoglobin Appearing after Severe Haemolysis: α2 minus 141 Arg β2

H. Lehmann, D. Beale, H. Marti, 1967 .

MAPPING OF ANTIGENIC SITES ON HUMAN HAEMOGLOBIN BY MEANS OF MONOCLONAL ANTIBODIES AND HAEMOGLOBIN VARIANTS

G. Stamatoyannopoulos, T. Papayannopoulou, H. Lehmann, 1981, The Lancet.

Residue 122 of sperm whale and horse myoglobin

H. Lehmann, A. Herrera, 1974 .

Storage of Red Cells for Blood-grouping after Freezing in Liquid Nitrogen

H LEHMANN, R G HUNTSMAN, B A HURN, 1960, British medical journal.

Haemoglobin F Texas II (α2γ26 Glu→Lys), the Second of the Haemoglobin F Texas Variants

H. Lehmann, P. Lorkin, R. Huntsman, 1968 .

Haemoglobin F Texas I (α2γ25Glu→Lys): a Variant of Haemoglobin F

H. Lehmann, D. Beale, G. Huntsman, 1967 .

Further characterization of haemoglobin F hull γ121 glutamic acid → lysine; γ136 alanine

H. Lehmann, B. Wiltshire, E. Ahern, 1973 .

Further characterisation of haemoglobin F Texas I: γ5 glutamic acid → lysine; γ136 alanine

H. Lehmann, B. Wiltshire, E. Ahern, 1972 .

Haemoglobin Norfolk in Nepali Gorkhas

H. Lehmann, S. Gupta, T. Mehrotra, 1975, Humangenetik.

Haemoglobin G norfolk: α 85 (F6) Asp → Asn

H. Lehmann, F. Vella, P. Darbre, 1975 .

Haemoglobin Warwickshire (beta 5 [A2] Pro----Arg). A possible 'fine tuning' of 2,3-DPG affinity by beta 5 Pro.

K. Imai, H. Lehmann, C. Wilson, 1984, FEBS letters.

Haemoglobin Warwickshire (β5 [A2] Pro → Arg)

K. Imai, H. Lehmann, R. J. Cave, 1984 .

Haemoglobin G Copenhagen and haemoglobin J Cambridge. Two new beta-chain variants of haemoglobin A.

D. Irvine, H. Lehmann, D. Beale, 1967, Biochimica et biophysica acta.

Familial polycythaemia caused by a new haemoglobin variant: Hb Heathrow, beta 103 (G5) phenylalanine leads to leucine.

H. Lehmann, J. White, I. Gillies, 1973, British medical journal.

Red Cell Antigens and Enzymes after Storage at −196°C, −100°C and −78°C

H. Lehmann, R. Huntsman, B. Hurn, 1961 .

The Unstable Hb Genova (β28Leu→Pro) in an East African Family

H. Lehmann, B. Wiltshire, Alexander Kendall, 1979 .

A new unstable haemoglobin: Hb Buenos Aires, beta 85 (F1) Phe leads to Ser.

H. Lehmann, J. White, B. Wiltshire, 1973, Acta haematologica.

Hemoglobin UBE-2 (α68 ASN→ASP) Observed in a Turkish Family

H. Lehmann, A. Arcasoy, A. Bilginer, 1984 .

Hemoglobin Duarte: (a2fl?2?"#{176}?0):A New Unstable Hemoglobin With Increased Oxygen Affinity

E. Beutler, H. Lehmann, A. Lang, 1974 .

Myoglobin of the orangutan as a phylogenetic enigma

A. Friday, H. Lehmann, O. Castillo, 1976, Nature.

A new haemoglobin J from Turkey ‐ HB Ankara (β 10 (A7) Ala → Asp).

H. Lehmann, A. Çavdar, A. Arcasoy, 1974 .

The oxygen affinity of haemoglobin St. Luke's

H. Lehmann, P. Lorkin, R. Casey, 1974, FEBS letters.

Haemoglobin Korle-Bu (1373 Aspartic Acid >Asparagine) Showinga One of the Two Amino Acid Substitutions of Haemoglobin C Harlem

H. Lehmann, B. Ringelhann, F. Konotey-Ahulu, 2006 .

Haemoglobin Osu-Christiansborg: a new β-chain variant of haemoglobin A (β52 (D3) aspartic acid → asparagine) in combination with haemoglobin S.

H. Lehmann, J. Kinderlerer, B. Ringelhann, 1971 .

Structural identification of haemoglobin F Kuala Lumpur: α2γ2 22(B4) Asp → Gly; 136 Ala

H. Lehmann, L. Lie-injo, B. Wiltshire, 1973 .

Haemoglobin Denmark Hill 95 (G2) Pro-Ala, a variant with unusual electrophoretic and oxygen-binding properties.

H. Lehmann, P. Lorkin, B. Wiltshire, 1972, Biochimica et biophysica acta.

Haemoglobin J Rajappen; 90 (FG2) Lys leads to Thr.

H. Lehmann, J. Kinderlerer, R. Hyde, 1971, Biochimica et biophysica acta.

The myoglobin of primates. VIII. Gorilla gorilla beringei (eastern highland gorilla).

H. Lehmann, D. Fossey, A. Romero‐Herrera, 1975, Biochimica et biophysica acta.

A new haemoglobin J-habana-α71(E20) alanine→glutamic acid

H. Lehmann, B. Colombo, H. Vidal, 1974 .

Haemoglobin J Nyanza: 21 (B2) Ala-Asp.

H. Lehmann, A. Lang, R. Barr, 1973, Biochimica et biophysica acta.

Haemoglobin·Indonesia (α 116 Glu → Lys) in an Italian Family

H. Lehmann, E. Gallo, G. Sansone, 1970 .

Haemoglobin L Persian Gulf: α57 (E6) Glycine → Arginine

H. Lehmann, S. Rahbar, J. Kinderlerer, 1969 .

Haemoglobin D-beta Los Angeles (D Punjab, alpha-2-beta-2 121 Glu NH2) in a Thai family.

H. Lehmann, D. Beale, S. Na-nakorn, 1968, Acta haematologica.

Urinary excretion of acid muco-polysaccharide in sibs with Morquio's syndrome and Reilly's granules in leucocytes.

H. Lehmann, N. Matsaniotis, C. Kattamis, 1967, Archives of disease in childhood.

Blood groups and enzymes of human red cells after five years' storage in liquid nitrogen.

H. Lehmann, R. Huntsman, B. Hurn, 1962, British medical journal.

HÆmoglobin D Punjab in a European Family in Australia

H. Lehmann, G. R. Anderson, B. Wiltshire, 1973, The Medical journal of Australia.

A Hb J cape town homozygote — association of Hb J cape town and alpha‐thalassaemia

H. Lehmann, M. Botha, D. Plowman, 1978, FEBS letters.

The myoglobin of the fruit-bat (Rousettus aegyptiacus).

H. Lehmann, O. Castillo, 1977, Biochimica et biophysica acta.

The myoglobin of primates. VI. Tupaia glis belangeri (common treeshrew).

H. Lehmann, A. Romero‐Herrera, 1974, Biochimica et Biophysica Acta.

The myoglobin of primates: Symphalangus syndactylus (SIAMANG)

H. Lehmann, O. Castillo, E. J. Bruce, 1977, FEBS letters.